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43. Using sex-averaged genetic maps in multipoint linkage analysis when identity-by-descent status is incompletely known. Fingerlin TE; Abecasis GR; Boehnke M Genet Epidemiol; 2006 Jul; 30(5):384-96. PubMed ID: 16685713 [TBL] [Abstract][Full Text] [Related]
44. Recurrence risks in an oligogenic threshold model: the effect of alterations in allele frequency. Kendler KS; Kidd KK Ann Hum Genet; 1986 Jan; 50(1):83-91. PubMed ID: 3426150 [TBL] [Abstract][Full Text] [Related]
45. Social selection in human populations: differential modification of the fitness by the sex of an affected parent. Yokoyama S J Theor Biol; 1984 Aug; 109(3):453-9. PubMed ID: 6471876 [TBL] [Abstract][Full Text] [Related]
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47. [DNA polymorphism and genetic diseases]. Baiget M Med Clin (Barc); 1986 May; 86(18):774-7. PubMed ID: 3526011 [No Abstract] [Full Text] [Related]
48. 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; 12(6):565-70. PubMed ID: 8787974 [TBL] [Abstract][Full Text] [Related]
50. Linkage analysis of two-locus diseases under single-locus and two-locus analysis models. Vieland V; Greenberg DA; Hodge SE; Ott J Cytogenet Cell Genet; 1992; 59(2-3):145-6. PubMed ID: 1737484 [No Abstract] [Full Text] [Related]
51. Age structure and the distribution of rare genetic diseases. Yokoyama S; Ward RH Am J Med Genet; 1984 Sep; 19(1):65-79. PubMed ID: 6496573 [TBL] [Abstract][Full Text] [Related]
52. Power and type I error in affected sib-pair methods under restricted estimation conditions. Dawson DV; Kaplan EB Prog Clin Biol Res; 1989; 329():189-94. PubMed ID: 2622952 [No Abstract] [Full Text] [Related]
53. [Genetic approaches to the study of human chronic diseases]. Bochkov NP; Ginter EK Ter Arkh; 1981; 53(11):3-6. PubMed ID: 7339900 [No Abstract] [Full Text] [Related]
54. Introduction to SNPs: discovery of markers for disease. Weiner MP; Hudson TJ Biotechniques; 2002 Jun; Suppl():4-7, 10, 12-3. PubMed ID: 12083396 [No Abstract] [Full Text] [Related]
55. Linkage analysis in nuclear families. 1: Optimality criteria for affected sib-pair tests. Knapp M; Seuchter SA; Baur MP Hum Hered; 1994; 44(1):37-43. PubMed ID: 8163290 [TBL] [Abstract][Full Text] [Related]
56. Mutation-selection balance with multiple alleles. Clark AG Genetica; 1998; 102-103(1-6):41-7. PubMed ID: 9720270 [TBL] [Abstract][Full Text] [Related]
60. Uniparental disomy as the basis for an association of rare disorders. Nicholls RD Am J Med Genet; 1991 Nov; 41(2):273-4. PubMed ID: 1785652 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]