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Longer titles found: Genetic Testing and Molecular Biomarkers (view), Point-of-care genetic testing (view)

searching for Genetic testing 118 found (1868 total)

Women's Hospital International and Fertility Centre (1,750 words) [view diff] case mismatch in snippet view article find links to article

integrates Genetic Screening and Diagnosis, including Preimplantation Genetic Testing (PGT), Preimplantation Genetic Diagnosis (PGD), and Preimplantation

Tricho-rhino-phalangeal syndrome Type 1 (524 words) [view diff] exact match in snippet view article find links to article

identification of characteristic physical features, and radiographic findings. Genetic testing can confirm mutations in the TRPS1 gene. Treatment of TRPS I is symptomatic

Ectodermal dysplasia (2,120 words) [view diff] exact match in snippet view article find links to article

dental and hair abnormalities, and characteristic facial features. Genetic testing can confirm the diagnosis, especially when there is a family history

Refsum disease (1,516 words) [view diff] exact match in snippet view article find links to article

tests showing above average serum levels of phytanic acid, or through genetic testing. Individuals with Refsum disease present with neurologic damage, cerebellar

Methylmalonic acidemias (4,446 words) [view diff] exact match in snippet view article find links to article

B12 responsiveness. The final diagnosis is confirmed by molecular genetic testing if biallelic pathogenic variants are found in the affected gene(s)

Bytadosi (1,609 words) [view diff] exact match in snippet view article find links to article

Petrov is believed to have been a descendant of the Crnojević dynasty. Genetic testing has confirmed that the Bekaj brotherhood is indeed related to the neighboring

Popliteal pterygium syndrome (1,211 words) [view diff] exact match in snippet view article find links to article

(PPS) can be diagnosed prenatally through ultrasound and confirmed via genetic testing. Ultrasound imaging can identify characteristic physical anomalies

Interstitial lung disease (2,996 words) [view diff] no match in snippet view article find links to article

Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD), is a group of respiratory diseases affecting the interstitium (the tissue)

Retinoblastoma (4,829 words) [view diff] case mismatch in snippet view article find links to article

PMID 9544909. Retinoblastoma information from MedlinePlus retinoblastoma at NIH/UW GeneTests RB1 Mutation Database NCBI Genetic Testing Registry

Theory of Kashmiri descent from lost tribes of Israel (375 words) [view diff] exact match in snippet view article find links to article

that the Kashmiri people originally descended from the Lost Tribes. Genetic testing and historical analysis have disproved this theory, meanwhile there

Genzyme (2,024 words) [view diff] no match in snippet view article find links to article

approximately 65 countries, including 17 manufacturing facilities and 9 genetic-testing laboratories. Its products were also sold in 90 countries. In 2007

McKusick–Kaufman syndrome (1,845 words) [view diff] exact match in snippet view article find links to article

have been linked to a pathogenic phenotype. There are advancements in genetic testing, that have improved the diagnostic accuracy, such as multigene panels

22q13 deletion syndrome (4,022 words) [view diff] exact match in snippet view article find links to article

Human Phenotype Browser search for 'hypotonia' and the OMIM database). Genetic testing is necessary to confirm the diagnosis of PMS. A prototypical terminal

DNAPrint Genomics (1,913 words) [view diff] exact match in snippet view article find links to article

difficult to identify. Autosomal DNA testing is a specific type of genetic testing that is done by looking at a subset of DNA regions in the autosomal

Érika Coimbra (322 words) [view diff] exact match in snippet view article find links to article

Volleyball Women's World Cup. She is a free agent. Coimbra passed all genetic testing required by the FIVB and the International Olympic Committee to play

Melungeon (4,221 words) [view diff] no match in snippet view article find links to article

Melungeon (/məˈlʌndʒən/ mə-LUN-jən) (sometimes also spelled Malungean, Melangean, Melungean, Melungin) was a slur historically applied to individuals and

Neonatal diabetes (2,757 words) [view diff] no match in snippet view article find links to article

Neonatal diabetes mellitus (NDM) is a disease that affects an infant and their body's ability to produce or use insulin. NDM is a kind of diabetes that

Stargardt disease (2,918 words) [view diff] exact match in snippet view article find links to article

examination were found to be misdiagnosed when subsequent genetic testing was done. Genetic testing can be utilized to ensure a proper diagnosis for which

Ankylosing spondylitis (5,972 words) [view diff] no match in snippet view article find links to article

Ankylosing spondylitis (AS) is a type of arthritis from the disease spectrum of axial spondyloarthritis. It is characterized by long-term inflammation

Rowton, Shropshire (1,085 words) [view diff] no match in snippet view article find links to article

Rowton is a small village in the Telford and Wrekin Borough, Shropshire, England. It is located seven miles north-west of Wellington. The area is a Chapelry

State privacy laws of the United States (902 words) [view diff] exact match in snippet view article find links to article

California Legislative Information (October 7, 2021). "SB-41 Privacy: genetic testing companies". Harrell, Heather (2016). "Biobanking Research and Privacy

Kenneth Blum (1,769 words) [view diff] exact match in snippet view article find links to article

exists to justify such a concept. He holds multiple patents relating to genetic testing and treatment for the supposed syndrome that have been licensed through

Genetic predisposition (1,786 words) [view diff] exact match in snippet view article find links to article

issue. Upon diagnosing individuals with particular conditions via genetic testing, their genetic predisposition can be measured with pedigree trees.

Aleutian wild cattle (260 words) [view diff] exact match in snippet view article find links to article

approximately 2,000 cattle on the island. Their origins are not known; genetic testing shows them to be genetically distinct from common American commercial

Designer baby (9,030 words) [view diff] case mismatch in snippet view article find links to article

Based on the specific analysis conducted: PGT-M (Preimplantation Genetic Testing for monogenic diseases) is a technique used during IVF to detect hereditary

Anne Wojcicki (2,001 words) [view diff] case mismatch in snippet view article find links to article

web}}: CS1 maint: numeric names: authors list (link) 23andMe. "DNA Genetic Testing & Analysis - 23andMe". www.23andme.com. Archived from the original

Poitevin horse (3,688 words) [view diff] no match in snippet view article find links to article

The Poitevin (French pronunciation: [pwat(ə)vɛ̃]) or Poitou is a French breed of draft horse. It is named for its area of origin, the former province of

1628 in Sweden (294 words) [view diff] exact match in snippet view article find links to article

2004 identified 15 adults and remains of at least two others. Further genetic testing will reveal more about the Vasa's crew. Foundation of the Lantmäteriet

Hereditary nonpolyposis colorectal cancer (5,044 words) [view diff] exact match in snippet view article find links to article

MSH6, and PMS2) or the EPCAM gene, identified by genetic testing. Candidates for germline genetic testing can be identified by clinical criteria such as

Demasduit (1,605 words) [view diff] no match in snippet view article find links to article

Demasduit (c. 1796 – January 8, 1820) was a Beothuk woman, one of the last of her people on Newfoundland. Demasduit was born around 1796, near the end

Nonosabasut (1,214 words) [view diff] no match in snippet view article find links to article

Nonosabasut (died March 1819) was a leader of the Beothuk people. He was the head of a family and partner of Demasduit, and was born on the island of Newfoundland

Succinate dehydrogenase complex subunit C (2,178 words) [view diff] exact match in snippet view article find links to article

Rodríguez-Antona C, Robledo M (September 2009). "Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma"

Monosomy (336 words) [view diff] exact match in snippet view article find links to article

occurrence in early developing embryos as demonstrated in preimplantation genetic testing. Mol Cytogenet. 2022 Mar 21;15(1):11. doi: 10.1186/s13039-022-00582-5

EMX2 (948 words) [view diff] case mismatch in snippet view article find links to article

1460-2075.1992.tb05284.x. PMC 556692. PMID 1376248. "Schizencephaly". Genetic Testing Registry (GTR). National Center for Biotechnology Information, U.S

Methyltransferase (2,919 words) [view diff] case mismatch in snippet view article find links to article

N-methyltransferase". NCBI Genetic Testing Registry. Retrieved 18 February 2014. "HNMT histamine N-methyltransferase". NCBI Genetic Testing Registry. Retrieved

× Sorbaronia fallax (339 words) [view diff] exact match in snippet view article find links to article

artificial hybrid between Aronia melanocarpa and Sorbus aucuparia. Before genetic testing, it was thought to be a hybrid among cultivars of Aronia melanocarpa

AARS2 (1,533 words) [view diff] exact match in snippet view article find links to article

findings are critical for diagnosis. Diagnostic confirmation involves genetic testing to identify pathogenic variants in AARS2. Whole exome sequencing (WES)

Bighorn sheep (3,981 words) [view diff] exact match in snippet view article find links to article

14 kg (30 lb); the sheep typically weigh up to 143 kg (315 lb). Recent genetic testing indicates three distinct subspecies of Ovis canadensis, one of which

Mostafa Ronaghi (617 words) [view diff] exact match in snippet view article find links to article

co-founded ParAllele BioScience to develop this multiplexed technology for genetic testing. ParAllele was acquired by Affymetrix in May 2005. In 2005, he co-founded

Hexanchiformes (1,622 words) [view diff] exact match in snippet view article find links to article

confirmed: Genetic testing finds a different sixgill shark". ScienceDaily. Retrieved 2020-08-21. "New species of shark discovered through genetic testing". phys

Island spotted skunk (1,593 words) [view diff] no match in snippet view article find links to article

The island spotted skunk (Spilogale gracilis amphiala) is an insular endemic carnivore and a subspecies of the western spotted skunk (Spilogale gracilis)

GeneReviews (190 words) [view diff] exact match in snippet view article find links to article

Bird, Thomas D.; Popovich, Bradley (2002). "GeneTests-GeneClinics: Genetic testing information for a growing audience". Human Mutation. 19 (5): 501–9

Human Fertilisation and Embryology Act 1990 (2,394 words) [view diff] no match in snippet view article find links to article

The Human Fertilisation and Embryology Act 1990 (c. 37) is an Act of the Parliament of the United Kingdom. It created the Human Fertilisation and Embryology

Branchio-oto-renal syndrome (1,189 words) [view diff] exact match in snippet view article find links to article

characterization, mutation distribution, and prospects for genetic testing". Genetic Testing. 1 (4): 243–251. doi:10.1089/gte.1997.1.243. PMID 10464653

Nonsyndromic deafness (1,853 words) [view diff] exact match in snippet view article find links to article

for visible abnormalities or signs of underlying conditions. Genetic testing: Genetic testing may be recommended, especially if there is a family history

Haplogroup R-DF27 (575 words) [view diff] no match in snippet view article find links to article

In human genetics, Haplogroup R-DF27 (R1b1a2a1a2a) is a Y-chromosome haplogroup which is a subdivision of haplogroup R-M269 (more specifically, its subclade

Turkification (8,054 words) [view diff] no match in snippet view article find links to article

Turkification, Turkization, or Turkicization (Turkish: Türkleştirme) describes a shift whereby populations or places receive or adopt Turkic attributes

Susan Michie (1,373 words) [view diff] exact match in snippet view article find links to article

genetic testing, informed choice and decision making about prenatal screening and genetic testing, and the psychological impact of predictive genetic

Wolfram syndrome (5,032 words) [view diff] exact match in snippet view article find links to article

of Wolfram syndrome is multifaceted, involving clinical evaluation, genetic testing, laboratory investigations, and imaging studies. Clinical evaluation

Cytochrome b5 reductase (3,135 words) [view diff] case mismatch in snippet view article find links to article

00043-3. ISBN 978-0-323-35762-3. "CYB5R1 cytochrome b5 reductase 1 - NIH Genetic Testing Registry (GTR) - NCBI". ncbi.nlm.nih.gov. Archived from the original

Biorepository (906 words) [view diff] exact match in snippet view article find links to article

and Prevention (CDC) Genetic Testing Reference Material Program (GeT-RM) maintains DNA samples for use in molecular genetic testing. These samples are from

Combined malonic and methylmalonic aciduria (3,261 words) [view diff] exact match in snippet view article find links to article

vitamin B12 in vivo. The final diagnosis is confirmed by molecular genetic testing if biallelic pathogenic variants are found in ACSF3 gene. There are

Salla disease (1,022 words) [view diff] exact match in snippet view article find links to article

by identifying genetic mutation(s) in the SLC17A5 gene by molecular genetic testing. This testing is available on a clinical basis. There is no cure for

KRT27 (94 words) [view diff] case mismatch in snippet view article find links to article

Information, U.S. National Library of Medicine. "KRT27 keratin 27 - NIH Genetic Testing Registry (GTR) - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2023-06-25

Leber congenital amaurosis (1,749 words) [view diff] exact match in snippet view article find links to article

(December 2007). "Leber congenital amaurosis - a model for efficient genetic testing of heterogeneous disorders: LXIV Edward Jackson Memorial Lecture".

Spondyloarthritis (5,897 words) [view diff] exact match in snippet view article find links to article

diagnosed based on symptoms and imaging. Early diagnosis criteria use genetic testing and more advanced forms of medical imaging. Spondyloarthritis is categorized

Rob Elles (197 words) [view diff] case mismatch in snippet view article find links to article

Co-operation and Development's guidelines for quality assurance in molecular Genetic Testing. He was chair of the British Society for Human Genetics from 2007 to

Lev's disease (2,738 words) [view diff] no match in snippet view article find links to article

Lev's disease, also known as Lenègre disease, is an idiopathic disease that can result in a complete heart block, or an extremely slowed heart rate, in

Osteogenesis imperfecta (15,404 words) [view diff] exact match in snippet view article find links to article

tomography. OI can also be detected before birth by using an in vitro genetic testing technique such as amniocentresis. In order to determine whether osteogenesis

Recurrent miscarriage (5,535 words) [view diff] exact match in snippet view article find links to article

of cases, the exact cause of pregnancy loss is unexplained despite genetic testing and a thorough evaluation. When a cause for RPL is identified, almost

Dor Yeshorim (1,319 words) [view diff] exact match in snippet view article find links to article

girls rap on genetic testing in viral video". The Times of Israel. Retrieved 2016-05-22. "WATCH: Orthodox girls rap on genetic testing in viral video"

Chromosome 7 (2,949 words) [view diff] case mismatch in snippet view article find links to article

2011.1. PMC 3709024. PMID 22241104. Gilbert F (2002). "Chromosome 7". Genetic Testing. 6 (2): 141–161. doi:10.1089/10906570260199429. PMID 12215256. Hillier

Cow shark (827 words) [view diff] exact match in snippet view article find links to article

shark species confirmed: Genetic testing finds a different sixgill shark". "New species of shark discovered through genetic testing". ReefQuest Centre: Order

D-Glyceric acidemia (380 words) [view diff] exact match in snippet view article find links to article

GLYCTK gene) OMIM [2] (information on GLYCTK gene, encoding Glycerate Kinase) GeneTests [3] (information on genetic testing for D-Glyceric Acidemia)

Renal cysts and diabetes syndrome (528 words) [view diff] exact match in snippet view article find links to article

as well, such as in 17q12 microdeletion syndrome.[citation needed] Genetic testing for mutations on the HNF1B gene can indicate MODY 5. The presence of

Tumor marker (1,850 words) [view diff] case mismatch in snippet view article find links to article

Promoting Safe and Effective Genetic Testing in the United States: Final Report of the Task Force on Genetic Testing. Johns Hopkins University Press

Hyper-IgM syndrome type 3 (675 words) [view diff] exact match in snippet view article find links to article

Hyper-IgM syndrome type 1,2,3,4 and 5 Diagnostic method MRI, Chest radiography and genetic testing Treatment Allogeneic hematopoietic cell transplantation

CDKL5 (2,256 words) [view diff] exact match in snippet view article find links to article

vary widely, and cases have been reported in both males and females. Genetic testing for CDKL5 is recommended in infants presenting with epileptic encephalopathy

Clan Pollock (804 words) [view diff] case mismatch in snippet view article find links to article

Pollock". 15 June 2020. Retrieved 26 March 2023. "FamilyTreeDNA - Genetic Testing for Ancestry, Family History & Genealogy". www.familytreedna.com. Retrieved

Multiple myeloma (13,208 words) [view diff] no match in snippet view article find links to article

Multiple myeloma (MM), also known as plasma cell myeloma and simply myeloma, is a cancer of plasma cells, a type of white blood cell that normally produces

Len Tepper (1,088 words) [view diff] exact match in snippet view article find links to article

Scheduled Newscast for Wounded Warrior, the 2017 Edward R Murrow for Genetic testing Gold Rush, and the 2017 Emmy for Investigative Report in a regular

Thyroid dyshormonogenesis (469 words) [view diff] exact match in snippet view article find links to article

release after perchlorate administration, which can be confirmed by genetic testing. Levothyroxine is the treatment of choice (starting dose 10-15 mcg/kg/day)

PURA syndrome (1,396 words) [view diff] exact match in snippet view article find links to article

the profound neurological phenotype. Diagnosis is confirmed through genetic testing and management remains supportive. Patients (usually children, but

Lymphedema–distichiasis syndrome (729 words) [view diff] exact match in snippet view article find links to article

Paolacci, Stefano; Marinelli, Carla; Bertelli, Matteo (2018-09-01). "Genetic testing for lymphedema-distichiasis syndrome". The EuroBiotech Journal. 2 (s1):

National Association of Testing Authorities (566 words) [view diff] case mismatch in snippet view article find links to article

Commonwealth of Australia. Retrieved 14 September 2019. "Regulating Access to Genetic Testing-Laboratory accreditation". Australian Law Reform Commission. Archived

SDHD (2,718 words) [view diff] exact match in snippet view article find links to article

Rodríguez-Antona C, Robledo M (September 2009). "Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma"

Domestication of the cat (2,226 words) [view diff] case mismatch in snippet view article find links to article

inactive as of November 2024 (link) Lyons, Leslie (December 2012). "Genetic Testing in Domestic Cats". National Institute's of Health. PMID 22546621. "Felis

Gigantiform cementoma (2,053 words) [view diff] exact match in snippet view article find links to article

regulation and cell signaling. With the new research there can be genetic testing done for diagnosis. This can help with early detection, close monitoring

SLC13A5 citrate transporter disorder (861 words) [view diff] exact match in snippet view article find links to article

patterns. Diagnosis is suspected based on symptoms and confirmed by genetic testing. Individuals with SLC13A5 Epilepsy require an accurate diagnosis to

Familial thoracic aortic aneurysm (549 words) [view diff] exact match in snippet view article find links to article

through a combination of clinical evaluation, imaging studies, and genetic testing. Patients especially those with a relevant family history are typically

Turner syndrome (9,458 words) [view diff] exact match in snippet view article find links to article

possibly none occur at all. Diagnosis is based on physical signs and genetic testing. No cure for Turner syndrome is known. Treatment may help with symptoms

Hexanchus (830 words) [view diff] exact match in snippet view article find links to article

Genetic testing finds a different sixgill shark". ScienceDaily. Retrieved 7 February 2019. "New species of shark discovered through genetic testing"

KIF6 (565 words) [view diff] case mismatch in snippet view article find links to article

case-control study of coronary artery disease in Western Indians". Genetic Testing and Molecular Biomarkers. 15 (12): 883–6. doi:10.1089/gtmb.2011.0079

Mitochondrial encephalomyopathy (1,726 words) [view diff] exact match in snippet view article find links to article

damage. Throughout the past 10 years, there have been major advances in genetic testing, which have transformed how mitochondrial disorders are diagnosed.

Paul J. Turek (2,433 words) [view diff] no match in snippet view article find links to article

Dr. Paul J Turek (born July 8, 1960, Manchester, Connecticut) is an American physician and surgeon, men's reproductive health specialist, and businessman

Epidermolytic hyperkeratosis (611 words) [view diff] exact match in snippet view article find links to article

these are unaffected. Diagnosis is by its appearance, skin biopsy, and genetic testing. The condition can be diagnosed via exam that reveals; generalized

Haplogroup Q-M242 (13,527 words) [view diff] case mismatch in snippet view article find links to article

PMID 21674832. "Family Tree DNA – Genetic Testing for Ancestry, Family History & Genealogy". "Family Tree DNA – Genetic Testing for Ancestry, Family History

Beare–Stevenson cutis gyrata syndrome (483 words) [view diff] exact match in snippet view article find links to article

craniosynostosis syndromes is based on clinical findings; molecular genetic testing of FGFR1, FGFR2, and FGFR3 may be helpful in establishing the specific

Dystrophinopathy (169 words) [view diff] exact match in snippet view article find links to article

dystrophy, Becker muscular dystrophy, DMD-associated dilated cardiomyopathy Causes Genetic (inherited or new mutation) Diagnostic method Genetic testing

SDHB (2,957 words) [view diff] exact match in snippet view article find links to article

malignant catecholamine-producing paragangliomas: implications for genetic testing". J. Clin. Endocrinol. Metab. 91 (11): 4505–9. doi:10.1210/jc.2006-0423

Acatalasia (412 words) [view diff] case mismatch in snippet view article find links to article

blood (acatalasaemia); report of nine cases". Lancet. 2 (6745): 1101–4. doi:10.1016/s0140-6736(52)90939-2. PMID 12991731. MedGen Genetic Testing Registry

GJC3 (708 words) [view diff] case mismatch in snippet view article find links to article

are not a major cause of nonsyndromic hearing impairment in India". Genetic Testing and Molecular Biomarkers. 14 (4): 539–41. doi:10.1089/gtmb.2010.0026

Mycosarcoma (216 words) [view diff] exact match in snippet view article find links to article

The six recognized species were in different genera originally until genetic testing showed their relations and they were reclassified as Mycosarcoma. Mycosarcoma

PGT (125 words) [view diff] exact match in snippet view article find links to article

PokerGO Tour (founded 2021), an American poker tour Preimplantation genetic testing (see Preimplantation genetic diagnosis) Puccinia graminis f. sp. tritici

Hyper-IgM syndrome type 4 (688 words) [view diff] exact match in snippet view article find links to article

Hyper-IgM syndrome type 1,2,3,4 and 5 Diagnostic method MRI, Chest radiography and genetic testing Treatment Allogeneic hematopoietic cell transplantation

Catel–Manzke syndrome (105 words) [view diff] case mismatch in snippet view article find links to article

others): Highly arched eyebrow Joint stiffness Scoliosis Short stature Genetic Testing Currently there are only around 26 people in the world that are known

Pancreatic cancer (13,579 words) [view diff] exact match in snippet view article find links to article

cases rather than diagnosis. All those with pancreatic cancer require genetic testing as high risk oncogenic mutations may provide prognostic information

I-cell (1,467 words) [view diff] exact match in snippet view article find links to article

lysosomal enzyme activity that suggest I-Cell Disease, specialists perform genetic testing to identify any GNPTAB gene mutations. To identify specific mutations

Cutis (anatomy) (165 words) [view diff] case mismatch in snippet view article

ISBN 978-0-7020-2968-4, retrieved 2024-11-24 "Aplasia cutis congenita - NIH Genetic Testing Registry (GTR) - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2024-12-07

Genetic Information Nondiscrimination Act (1,629 words) [view diff] exact match in snippet view article find links to article

legislation does not go far enough in enabling personal control over genetic testing results. The law does not cover life, disability, or long-term care

Oncology (2,732 words) [view diff] exact match in snippet view article find links to article

S2CID 2544266. Katsanis, Sara Huston; Katsanis, Nicholas (2013). "Molecular genetic testing and the future of clinical genomics". Nat Rev Genet. 14 (6): 415–426

Gordon syndrome (947 words) [view diff] exact match in snippet view article find links to article

birth, such as clubfoot or cleft palate. Diagnosis is conducted by genetic testing to identify mutations in the PIEZO2 gene, and x-rays may be ordered

Eiken syndrome (476 words) [view diff] exact match in snippet view article find links to article

Diagnosis often includes clinical evaluation, radiographic imaging, and genetic testing to identify mutations that may be responsible for the syndrome. The

Cyclic nucleotide gated channel beta 3 (819 words) [view diff] exact match in snippet view article find links to article

S2CID 45853869. Koenekoop RK, Lopez I, den Hollander AI, et al. (2007). "Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutions"

Cyclic nucleotide gated channel beta 3 (819 words) [view diff] exact match in snippet view article find links to article

S2CID 45853869. Koenekoop RK, Lopez I, den Hollander AI, et al. (2007). "Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutions"

In vitro fertilisation (21,413 words) [view diff] exact match in snippet view article find links to article

enable gestational surrogacy, and, in combination with pre-implantation genetic testing, avoid the transmission of abnormal genetic conditions. When a fertilised

Hypercalciuria (653 words) [view diff] exact match in snippet view article find links to article

There can be an underlying genetic component that is beyond current genetic testing available. In familial cases it is common that 50% of first degree

Keratin 2A (1,107 words) [view diff] exact match in snippet view article find links to article

bullosa of Siemens: its correct diagnosis facilitated by molecular genetic testing". Br. J. Dermatol. 152 (6): 1353–6. doi:10.1111/j.1365-2133.2005.06598

Syncoilin (1,531 words) [view diff] case mismatch in snippet view article find links to article

M2-Polarized Macrophages in the Gastric Tumor Immune Microenvironment". Genetic Testing and Molecular Biomarkers. 25 (3): 236–246. doi:10.1089/gtmb.2020.0131

KIR2DS1 (705 words) [view diff] case mismatch in snippet view article find links to article

receptor (KIR) genotypes in patients with familial Mediterranean fever". Genetic Testing and Molecular Biomarkers. 13 (1): 91–5. doi:10.1089/gtmb.2008.0081

CYP2C19 (3,879 words) [view diff] case mismatch in snippet view article find links to article

community, the Centers for Disease Control and Prevention established the Genetic Testing Reference Material Program to meet the need for publicly available

New York State Task Force on Life and the Law (2,461 words) [view diff] exact match in snippet view article find links to article

allocation of organs for transplantation, surrogacy, medical aid-in-dying, genetic testing and screening, the allocation of ventilators in a pandemic, and research

Laura J. van 't Veer (972 words) [view diff] no match in snippet view article find links to article

genetic-testing-for-breast-cancer/ https://ascopost.com/issues/august-10-2019/how-laura-j-van-t-veer-phd-became-an-expert-in-genetic-testing-for-breast-cancer/

COLD-PCR (1,607 words) [view diff] exact match in snippet view article find links to article

COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing". Nature Medicine. 14 (5): 579–84. doi:10.1038/nm1708. PMID 18408729

Myosin-heavy chain myopathy (248 words) [view diff] exact match in snippet view article find links to article

with significant Quarter Horse bloodlines. It was added to the AQHA genetic testing panel in 2022. It is a genetic dominant condition, though not all horses

Hyper-IgM syndrome type 2 (716 words) [view diff] exact match in snippet view article find links to article

Hyper-IgM syndrome type 1,2,3,4 and 5 Diagnostic method MRI, Chest radiography and genetic testing Treatment Allogeneic hematopoietic cell transplantation

Amal dynasty (959 words) [view diff] case mismatch in snippet view article find links to article

Origin and Deeds of the Goths (Getica) Vadamerca "FamilyTreeDNA – Genetic Testing for Ancestry, Family History & Genealogy". FamilyTreeDNA. Retrieved

Vitelliform macular dystrophy (1,150 words) [view diff] case mismatch in snippet view article find links to article

Genetics Home Reference Best's disease - eMedicine.com GeneReviews/NCBI/NIH/UW entry on Best Vitelliform Macular Dystrophy NCBI Genetic Testing Registry