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Find link is a tool written by Edward Betts.searching for mutation testing 24 found (40 total)
alternate case: Mutation testing
Lightweight software test automation
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aspx. A technique for mutation testing using lightweight software test automation: "Mutant Power: Create a Simple Mutation Testing System with the .NETSack–Barabas syndrome (769 words) [view diff] exact match in snippet view article find links to article
collagen typing (performed on a skin biopsy sample) or collagen gene mutation testing. There is no cure for Ehlers-Danlos syndrome, so individual problemsGalactose-1-phosphate uridylyltransferase deficiency (1,282 words) [view diff] exact match in snippet view article find links to article
red blood cells, determination of Gal-1-P levels in the blood, and mutation testing. The differential diagnosis for elevated galactose concentrations inCDKN2D (1,227 words) [view diff] exact match in snippet view article find links to article
PMID 10208428. Newton Bishop JA, Harland M, Bennett DC, et al. (1999). "Mutation testing in melanoma families: INK4A, CDK4 and INK4D". Br. J. Cancer. 80 (1–2):CHARGE syndrome (1,581 words) [view diff] exact match in snippet view article find links to article
of 379 clinically diagnosed cases of CHARGE syndrome, in which CHD7 mutation testing was undertaken found that 67% of cases were due to a CHD7 mutationAge of onset (1,421 words) [view diff] case mismatch in snippet view article find links to article
PMID 13679864. Smith, Karen Lisa; Isaacs, Claudine (2011). "BRCA Mutation Testing in Determining Breast Cancer Therapy". The Cancer Journal. 17 (6):Lungscape (442 words) [view diff] exact match in snippet view article find links to article
results of a worldwide external quality assessment (EQA) scheme for EGFR mutation testing. Br J Cancer, 2014. 111(2): p. 413-20. Blackhall, F.H., et al., PrevalenceHenry T. Lynch (1,007 words) [view diff] case mismatch in snippet view article find links to article
"Family Information Service Participation Increases the Rates of Mutation Testing among Members of Families with BRCA1/2 Mutations". The Breast JournalPolycythemia (3,287 words) [view diff] exact match in snippet view article find links to article
morphology Iron panel to evaluate for concurrent iron deficiency JAK2 mutation testing Serum erythropoeitin (EPO) levels Oxygen saturation (usually via pulseOligodendroglioma (3,064 words) [view diff] exact match in snippet view article find links to article
"Diffuse gliomas in patients aged 55 years or over: A suggestion for IDH mutation testing". Neuropathology. 40 (1): 68–74. doi:10.1111/neup.12608. hdl:11380/1317437Spinal disease (3,054 words) [view diff] exact match in snippet view article find links to article
used for patients who "are negative for both SMN1 deletion and SMN1 mutation testing." As of right now, there are no successful treatments. However, manyLiquid biopsy (2,322 words) [view diff] exact match in snippet view article find links to article
2017). "The first liquid biopsy test approved. Is it a new era of mutation testing for non-small cell lung cancer?". Annals of Translational MedicineMethylenetetrahydrofolate reductase (3,877 words) [view diff] exact match in snippet view article find links to article
855–863. doi:10.4088/JCP.13m08947. PMID 24813065. "Dubious MTHFR genetic mutation testing". Science-Based Medicine. 2015-06-11. Retrieved 2018-07-13. HermesNon-small-cell lung cancer (5,603 words) [view diff] exact match in snippet view article find links to article
metastatic sites of advanced non-small-cell lung cancer and the impact of mutation testing methodologies: a literature review". Journal of Experimental & ClinicalMolecular diagnostics (4,589 words) [view diff] exact match in snippet view article find links to article
L, Hidalgo M, López-Ríos F (27 August 2012). "A comparison of EGFR mutation testing methods in lung carcinoma: direct sequencing, real-time PCR and immunohistochemistry"Code integrity (918 words) [view diff] exact match in snippet view article find links to article
Different types of code coverage (line-coverage, branch-coverage etc.) Mutation testing Advantages of shift-left code integrity Shorter development time -KRAS (5,085 words) [view diff] exact match in snippet view article find links to article
Sulżyc-Bielicka V, Cybulski C, Ryś J, Domagała W (November 2012). "KRAS mutation testing in colorectal cancer as an example of the pathologist's role in personalizedLesch–Nyhan syndrome (4,840 words) [view diff] exact match in snippet view article find links to article
negative outcomes. If only a suspected carrier female is available for mutation testing, it may be appropriate to grow her lymphocytes in 6-thioguanine (aInternet of things (20,188 words) [view diff] case mismatch in snippet view article find links to article
Mohsen; Kiaei, Pantea; Emamdoost, Navid (2021). SN4KE: Practical Mutation Testing at Binary Level (PDF) (MSc). NDSS Symposium 2021. Clearfield, ChristopherHigh-resolution melting analysis (2,581 words) [view diff] exact match in snippet view article find links to article
et al. (February 2006). "Optimal selection of individuals for BRCA mutation testing: a comparison of available methods". J. Clin. Oncol. 24 (4): 707–15Breast cancer screening (7,129 words) [view diff] case mismatch in snippet view article find links to article
33782. PMC 9290473. PMID 34460111. "Genetic Risk Assessment and BRCA Mutation Testing for Breast and Ovarian Cancer Susceptibility: Recommendation Statement"BRCA mutation (8,839 words) [view diff] case mismatch in snippet view article find links to article
Gelber S, Schapira L, Come S, et al. (June 2016). "BRCA1 and BRCA2 Mutation Testing in Young Women With Breast Cancer". JAMA Oncology. 2 (6): 730–736.Oncometabolism (3,430 words) [view diff] exact match in snippet view article find links to article
shown to be a useful diagnostic tool for prioritizing patients for SDH mutation testing in early stages of cancer. The absence of SDHB in IHC staining wouldGynecologic cancer disparities in the United States (4,770 words) [view diff] case mismatch in snippet view article find links to article
Miranda; Bougatsos, Christina (2005). Genetic Risk Assessment and BRCA Mutation Testing for Breast and Ovarian Cancer Susceptibility. Rockville (MD): Agency