Found: 7
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Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome.
- Published in:
- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 12, p. 1469
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- Article
A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A→C is a mutation.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 399, doi. 10.1007/s10038-003-0044-0
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- Article
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa.
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- Annals of Neurology, 2014, v. 75, n. 4, p. 525, doi. 10.1002/ana.24114
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- Article
Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 3, p. 309, doi. 10.1002/gcc.20189
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- Article
Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens.
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- European Journal of Human Genetics, 2012, v. 20, n. 1, p. 27, doi. 10.1038/ejhg.2011.134
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- Article
Bioinformatics and Human Identification in Mass Fatality Incidents: The World Trade Center Disaster.
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- Journal of Forensic Sciences, 2007, v. 52, n. 4, p. 806, doi. 10.1111/j.1556-4029.2007.00456.x
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- Article
Accurate STR Allele Designations at the FGA and vWa Loci Despite Primer Sute Polymorphisms.
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- Journal of Forensic Sciences, 2004, v. 49, n. 2, p. 250, doi. 10.1520/JFS2003192
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- Article