These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. The cis-trans effects of crossing-over on the penetrance and expressivity of dominantly inherited disorders. Côté GB. Ann Genet; 1989 Oct; 32(3):132-5. PubMed ID: 2817771 [Abstract] [Full Text] [Related]
6. A new strategy for linkage analysis under epistasis taking into account genetic heterogeneity. Bureau A, Mérette C, Croteau J, Fournier A, Chagnon YC, Roy MA, Maziade M. Hum Hered; 2009 Oct; 68(4):231-42. PubMed ID: 19622890 [Abstract] [Full Text] [Related]
7. Determining trait locus position from multipoint analysis: accuracy and power of three different statistics. Greenberg DA, Abreu PC. Genet Epidemiol; 2001 Dec; 21(4):299-314. PubMed ID: 11754466 [Abstract] [Full Text] [Related]
12. Statistical genetics of normal variation in family data for oligogenic diseases. Mahaney MC, Jaquish CE, Comuzzie AG. Genet Epidemiol; 1995 Mar; 12(6):783-7. PubMed ID: 8788009 [Abstract] [Full Text] [Related]
13. Use of sibling risk ratios and components of genetic variance in the characterization of a simulated oligogenic disease. Almasy L, Tierney C, Risch N. Genet Epidemiol; 1995 Mar; 12(6):565-70. PubMed ID: 8787974 [Abstract] [Full Text] [Related]