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Longer titles found: Online Mendelian Inheritance in Man (view), Non-Mendelian inheritance (view), The Correlation between Relatives on the Supposition of Mendelian Inheritance (view), Online Mendelian Inheritance in Animals (view)

searching for Mendelian inheritance 66 found (975 total)

alternate case: mendelian inheritance

Tracy Sonneborn (1,222 words) [view diff] no match in snippet view article find links to article

Tracy Morton Sonneborn ForMemRS (October 19, 1905 – January 26, 1981) was an American biologist. His life's study was ciliated protozoa of the group Paramecium

Oligogenic inheritance (1,121 words) [view diff] exact match in snippet view article find links to article

a mutation do not show the pattern of phenotypes expected under Mendelian inheritance, other models may better explain observed patterns of inheritance

Inflammatory bowel disease-22 (72 words) [view diff] case mismatch in snippet view article find links to article

Inflammatory bowel disease-22 is a human phenotype with Mendelian Inheritance in Man (MIM) symbol IBD22 and associated with genetic locus 17q21.2 on the

Allelic heterogeneity (463 words) [view diff] case mismatch in snippet view article find links to article

considered to be rare or exclusive to a single pedigree. The Online Mendelian Inheritance of Man has a record of over 1000 genes and their associated allelic

Heme transporter (1,009 words) [view diff] case mismatch in snippet view article find links to article

doi:10.1212/wnl.51.6.1772-a. PMID 9855554. S2CID 46553303. "Online Mendelian Inheritance in Man:FLCVR1". omim.org. GeneCard for FLVCR2 Duffy SP, Shing J

Jan Willem Moll (315 words) [view diff] exact match in snippet view article find links to article

associate of Hugo de Vries and his student Tine Tammes worked on Mendelian inheritance of quantitative traits. He developed both laboratory and field techniques

MEG3 (753 words) [view diff] exact match in snippet view article find links to article

region and results in the callipyge muscular hypertrophy. The non-Mendelian inheritance pattern, known as polar overdominance, likely results from the combination

Macrostomia (851 words) [view diff] case mismatch in snippet view article find links to article

S2CID 23100377. O'Neil, Marla. "Macrostomia, Isolated". Online Mendelian Inheritance in Men. Retrieved 8 November 2015. Fadeyibi, Idowu (20 December

Eponym (2,582 words) [view diff] case mismatch in snippet view article find links to article

[only] or Mendelian [only] mendelian inheritance [only] or Mendelian inheritance [only] but Mendel's laws *Mendelian Inheritance Newtonian [only] *newtonian

Isolated congenital asplenia (389 words) [view diff] case mismatch in snippet view article find links to article

ICAS, often causes meningitis, sepsis, and otitis media. Online Mendelian Inheritance in Man. OMIM entry 271400: Asplenia, isolated congenital; ICAS.

Gene Disease Database (4,135 words) [view diff] case mismatch in snippet view article find links to article

diseases such as the Comparative Toxicogenomics Database (CTD), Online Mendelian Inheritance in Man (OMIM), the genetic Association Database (GAD) or the Disease

Jared Roach (1,250 words) [view diff] case mismatch in snippet view article find links to article

(February 16, 2017). "DIHYDROOROTATE DEHYDROGENASE; DHODH". Online Mendelian Inheritance in Man (OMIM). National Library of Medicine. Retrieved February

Acromesomelic dysplasia (2,588 words) [view diff] case mismatch in snippet view article find links to article

Online Mendelian Inheritance in Man (OMIM). OMIM Entry - #602875. Retrieved 2020-11-09. "Chondrodysplasia, Grebe Type TYPE". Online Mendelian Inheritance in

Mary Isabel McCracken (543 words) [view diff] exact match in snippet view article find links to article

mosquitoes, silkworms, aphids, and bees, and was first to describe non-Mendelian inheritance as "purely maternal". McCracken also conducted field observation

Campine chicken (920 words) [view diff] case mismatch in snippet view article find links to article

Cytochrome P450, family 19, subfamily A, polypeptide 1; CYP19A1. Online Mendelian Inheritance in Man, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins

Amelanism (1,537 words) [view diff] case mismatch in snippet view article find links to article

300–19. doi:10.1034/j.1600-0749.2000.130502.x. PMID 11041206. Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM

The Monarch Initiative (546 words) [view diff] case mismatch in snippet view article find links to article

Phenotyping Consortium Mouse Phenome Database Online Mendelian Inheritance in Animals ClinVar Mendelian Inheritance in Man ORPHANET Protein ANalysis THrough Evolutionary

Glycerol kinase deficiency (2,009 words) [view diff] exact match in snippet view article find links to article

is a deletion or mutation of a single gene. GKD is described by Mendelian inheritance and is an X-linked recessive trait due to which it occurs mainly

Glycerol kinase deficiency (2,009 words) [view diff] exact match in snippet view article find links to article

is a deletion or mutation of a single gene. GKD is described by Mendelian inheritance and is an X-linked recessive trait due to which it occurs mainly

Aminocarboxymuconate-semialdehyde decarboxylase (262 words) [view diff] exact match in snippet view article find links to article

Garvin, Michael R. (2023). "Structural variants identified using non-Mendelian inheritance patterns advance the mechanistic understanding of autism spectrum

Leucism (921 words) [view diff] case mismatch in snippet view article find links to article

dominant white Archived 2009-01-30 at the Wayback Machine at Online Mendelian Inheritance in Animals. An L1 element intronic insertion in the black-eyed white

Ochratoxin (261 words) [view diff] case mismatch in snippet view article find links to article

200600137. PMID 17195275. "#261600 ICD+ PHENYLKETONURIA; PKU". Online Mendelian Inheritance in Man. Woolf, L. I. "The heterozygote advantage in phenylketonuria

Posterior polymorphous corneal dystrophy (236 words) [view diff] case mismatch in snippet view article find links to article

1007/BF01974655. "Posterior polymorphous corneal dystrophy". Online Mendelian Inheritance in Man(OMIM). Posterior Polymorphous Corneal Dystrophy at eMedicine

Mothers against decapentaplegic (182 words) [view diff] case mismatch in snippet view article find links to article

AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 4; SMAD4". Online Mendelian Inheritance in Man. Johns Hopkins University. January 18, 1996. Retrieved October

Trichorrhexis invaginata (1,012 words) [view diff] case mismatch in snippet view article find links to article

life-threatening infections, sepsis, and dehydration. The Netherton syndrome Mendelian Inheritance in Man is inherited as an autosomal recessive disorder due to mutations

TTC8 (634 words) [view diff] case mismatch in snippet view article find links to article

(2012-11-02). "OMIM entry #209900 Bardet-Biedl Syndrome; BBS". Online Mendelian Inheritance in Man. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins

Polled livestock (1,127 words) [view diff] case mismatch in snippet view article find links to article

Saltmarsh Ranch Soay Sheep). "Polled/Horns in Capra hircus". Online Mendelian Inheritance in Animals (OMIA). Retrieved 20 September 2021. Simon, R.; Lischer

CMTX2 (86 words) [view diff] case mismatch in snippet view article find links to article

Retrieved 2014-02-23. "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2; CMTX2". Online Mendelian Inheritance in Man. Retrieved 2024-10-17. v t e

Carney triad (520 words) [view diff] case mismatch in snippet view article find links to article

succinate dehydrogenase subunits SDHD, SDHC and SDHB. OMIM - Online Mendelian Inheritance in Man. Carney Triad (OMIM 604287) [1] Carney JA. "The triad of

Gene Wiki (1,032 words) [view diff] case mismatch in snippet view article find links to article

Nomenclature Committee – official gene name Entrez – Gene database OMIM (Mendelian Inheritance in Man) – database that catalogues all the known diseases with a

Chilodonella uncinata (1,407 words) [view diff] exact match in snippet view article find links to article

PMC 84415. PMID 10409752. T. Robinson & L. A. Katz (2007). "Non-Mendelian inheritance of paralogs of 2 cytoskeletal genes in the ciliate Chilodonella

Gustave Malécot (261 words) [view diff] case mismatch in snippet view article find links to article

article The Correlation Between Relatives on the Supposition of Mendelian Inheritance. Between 1940 and 1942, with France under Nazi German occupation

Glycogen branching enzyme (2,827 words) [view diff] case mismatch in snippet view article find links to article

Library of Medicine. "Glycogen Branching Enzyme; GBE1". Online Mendelian Inheritance in Man. Johns Hopkins University. Genetics Home Reference. "GBE1"

APOBEC (754 words) [view diff] case mismatch in snippet view article find links to article

mRNA-EDITING ENZYME, CATALYTIC POLYPEPTIDE 1; APOBEC1". Online Mendelian Inheritance in Man. Retrieved 23 December 2023. Blanc V, Davidson NO (January

Glycogen branching enzyme (2,827 words) [view diff] case mismatch in snippet view article find links to article

Library of Medicine. "Glycogen Branching Enzyme; GBE1". Online Mendelian Inheritance in Man. Johns Hopkins University. Genetics Home Reference. "GBE1"

Bussey Institution (311 words) [view diff] exact match in snippet view article find links to article

a pioneer in plant genetics, also worked there when he studied Mendelian inheritance. The geneticist William E. Castle worked there from 1908 until it

Posterior column ataxia-retinitis pigmentosa syndrome (222 words) [view diff] case mismatch in snippet view article find links to article

doi:10.1016/j.ajhg.2010.10.013. PMC 2978959. PMID 21070897. "Online Mendelian Inheritance in Man:FLCVR1". omim.org. Higgins JJ, Morton DH, Patronas N, Nee

Palmoplantar ectodermal dysplasia (102 words) [view diff] case mismatch in snippet view article find links to article

disease Ectodermal dysplasia McKusick, Victor A. (29 June 1998). Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders. JHU Press

Arterial calcification due to CD73 deficiency (250 words) [view diff] case mismatch in snippet view article find links to article

PMID 23122642. "Calcification of Joints and Arteries; CALJA". Online Mendelian Inheritance in Man. OMIM Entry - # 211800. Retrieved 19 June 2020. Kordaß T

Collagen, type XII, alpha 1 (944 words) [view diff] case mismatch in snippet view article find links to article

Type XII, Alpha-1; COL12A1 Gene-Phenotype Relationships". Online Mendelian Inheritance in Man. Oh SP, Taylor RW, Gerecke DR, Rochelle JM, Seldin MF, Olsen

Aspergum (564 words) [view diff] case mismatch in snippet view article find links to article

Section: Health; Page 1. Aspirin resistance, text MIM 608223, Online Mendelian Inheritance in Man Aspirin and Coronary Thrombosis Archived 11 July 2007 at

Human Protein Reference Database (813 words) [view diff] case mismatch in snippet view article find links to article

proteins involved in human diseases is annotated and linked to Online Mendelian Inheritance in Man (OMIM) database. The National Center for Biotechnology Information

1966 in science (1,292 words) [view diff] case mismatch in snippet view article find links to article

edition of his catalogue of all known genes and genetic disorders, Mendelian Inheritance in Man. Long-term potentiation (LTP), the putative cellular mechanism

Parkman, Maine (931 words) [view diff] case mismatch in snippet view article find links to article

Gate Bridge Victor A. McKusick, geneticist, original author of Mendelian Inheritance in Man database Vincent L. McKusick, chief justice of the Maine

Salix udensis (265 words) [view diff] exact match in snippet view article find links to article

Shield I, Macalpine W, Lindegaard K, Bayon C, Karp A (2010). "Mendelian inheritance of rust resistance to Melampsora larici‐epitea in crosses between

Evolution: The Modern Synthesis (733 words) [view diff] no match in snippet view article find links to article

including genetic variation, natural selection, and particulate (Mendelian) inheritance. This ended the eclipse of Darwinism and supplanted a variety of

KIAA1279 (650 words) [view diff] case mismatch in snippet view article find links to article

6 (5): 337–45. doi:10.1093/dnares/6.5.337. PMID 10574462. Online Mendelian Inheritance in Man entry on GOLDBERG-SHPRINTZEN MEGACOLON SYNDROME v t e

Supernumerary body part (903 words) [view diff] case mismatch in snippet view article find links to article

Polydactyl cat List of anatomical variations Caudal duplication Online Mendelian Inheritance in Man. "Nipples, Supernumerary". Accessed 10 July 2006. PatientPlus

Banki syndrome (288 words) [view diff] case mismatch in snippet view article find links to article

Retrieved 2021-03-20. McKusick, Victor Almon; Osler, William (1983). Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and

HOTHEAD (gene) (517 words) [view diff] exact match in snippet view article

Victor JL, Young JM, Pruitt RE (March 2005). "Genome-wide non-mendelian inheritance of extra-genomic information in Arabidopsis". Nature. 434 (7032):

HOTHEAD (gene) (517 words) [view diff] exact match in snippet view article

Victor JL, Young JM, Pruitt RE (March 2005). "Genome-wide non-mendelian inheritance of extra-genomic information in Arabidopsis". Nature. 434 (7032):

Kim Peek (1,708 words) [view diff] case mismatch in snippet view article find links to article

Smith JF, Santoro L (September 2008). "The FG syndromes (Online Mendelian Inheritance in Man 305450): perspective in 2008". Adv Pediatr. 55 (1): 123–70

DPP9 (973 words) [view diff] case mismatch in snippet view article find links to article

"Autoinflammation With Arthritis and Dyskeratosis; AIADK". Online Mendelian Inheritance in Man. 617388. Zhong FL, Robinson K, Teo DE, Tan KY, Lim C, Harapas

Irma Andersson-Kottö (426 words) [view diff] case mismatch in snippet view article find links to article

Andersson, Irma (1927). "Note on some characters in ferns subject to Mendelian Inheritance". Hereditas. 9 (1–3): 157–168. doi:10.1111/j.1601-5223.1927.tb03517

Robert Hibbs Peebles (452 words) [view diff] exact match in snippet view article find links to article

Research. 34 (10): 921–926. Peebles, R. H., & Kearney, T. H. 1928. Mendelian inheritance of leaf shape in cotton. Journal of Heredity, 19(5), 235–238. Kearney

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

2003), and the first to document an instance of meiotic drive, a Mendelian inheritance caused by preferential segregation of certain versions of homologous

Bioinformatic Harvester (621 words) [view diff] case mismatch in snippet view article find links to article

information hyperlinked over proteins via gene/protein synonyms Mendelian Inheritance in Man project catalogues all the known diseases RZPD, German resources

Membrane-associated transporter protein (1,335 words) [view diff] case mismatch in snippet view article find links to article

"OMIM Entry - #606574 - ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4". Mendelian Inheritance in Man. Johns Hopkins University. Retrieved 2020-08-05. Xu X, Dong

Timeline of plant pathology (569 words) [view diff] exact match in snippet view article find links to article

First chair of plant pathology established, in Copenhagen 1904; Mendelian inheritance of cereal rust resistance demonstrated 1907; First academic department

Pituitary-specific positive transcription factor 1 (1,372 words) [view diff] case mismatch in snippet view article find links to article

"POU DOMAIN, CLASS 1, TRANSCRIPTION FACTOR 1; POU1F1". Online Mendelian Inheritance in Man. Retrieved 3 January 2024. Bodner M, Castrillo JL, Theill

SATB1 (3,024 words) [view diff] case mismatch in snippet view article find links to article

PMID 33513338. "Den Hoed-De Boer-Voisin Syndrome; DHDBV". Online Mendelian Inheritance in Man (OMIM). Johns Hopkins University. Entry - #619229. Retrieved

White–Sutton syndrome (415 words) [view diff] case mismatch in snippet view article find links to article

intellectual disability" in January 2016. In June 2016, the Online Mendelian Inheritance in Man (OMIM) designated this as "White–Sutton syndrome". Reference

Woolly hair (1,008 words) [view diff] case mismatch in snippet view article find links to article

Human Genetics. Macmillan. p. 1355. McKusick, Victor Almon (1971). Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and

Uniparental disomy (1,146 words) [view diff] case mismatch in snippet view article find links to article

Disomy". Retrieved 29 February 2016. Angelman Syndrome, Online Mendelian Inheritance in Man "OMIM Entry - # 608149 - KAGAMI-OGATA SYNDROME". omim.org

TRIM32 (1,595 words) [view diff] case mismatch in snippet view article find links to article

(2012-11-02). "OMIM entry #209900 Bardet-Biedl Syndrome; BBS". Online Mendelian Inheritance in Man. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins

Booted eagle (2,224 words) [view diff] exact match in snippet view article find links to article

investigating polymorphism that these discrete colour morphs follow a Mendelian inheritance pattern, where the paler allele is dominant. In South Africa, 20%