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2. Linkage and association in complex genetic diseases. Sanders AR; Gershon ES Am J Psychiatry; 1997 Dec; 154(12):1640. PubMed ID: 9396939 [No Abstract] [Full Text] [Related]
3. From the tomato to the mouse. Marx J Science; 1990 Mar; 247(4950):1541. PubMed ID: 1969680 [No Abstract] [Full Text] [Related]
4. Dissecting the genetic component of complex diseases in humans. Reis A Ernst Schering Res Found Workshop; 2002; (38):1-15. PubMed ID: 12060997 [No Abstract] [Full Text] [Related]
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7. Evolving methods in genetic epidemiology. II. Genetic linkage from an epidemiologic perspective. Risch N Epidemiol Rev; 1997; 19(1):24-32. PubMed ID: 9360899 [No Abstract] [Full Text] [Related]
8. Molecular genetics of common diseases. Scott J Br Med J (Clin Res Ed); 1987 Sep; 295(6601):769-71. PubMed ID: 3119030 [No Abstract] [Full Text] [Related]
9. Overview of strategies for complex genetic diseases. Clerget-Darpoux F Kidney Int; 1998 Jun; 53(6):1441-5. PubMed ID: 9607171 [No Abstract] [Full Text] [Related]
10. The future of genetic studies of complex human diseases. Risch N; Merikangas K Science; 1996 Sep; 273(5281):1516-7. PubMed ID: 8801636 [No Abstract] [Full Text] [Related]
11. Genetic recombination and disease. Siniscalco M Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():191-4. PubMed ID: 3472715 [No Abstract] [Full Text] [Related]
12. 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]
13. Diseases determined by major genes. Morton NE Soc Biol; 1979; 26(2):94-103. PubMed ID: 550297 [No Abstract] [Full Text] [Related]
14. Genetic linkage as a cause of clinical variation in inherited disorders. Berg K Cytogenet Cell Genet; 1978; 22(1-6):618-20. PubMed ID: 752553 [No Abstract] [Full Text] [Related]
15. Analysis of linkage with disease-marker association. Tai JJ Proc Natl Sci Counc Repub China B; 1986 Oct; 10(4):250-3. PubMed ID: 3470816 [TBL] [Abstract][Full Text] [Related]
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17. NICHD conference. Genomic imprinting: consequences of uniparental disomy for human disease. Schinzel A Am J Med Genet; 1993 Jul; 46(6):683-4. PubMed ID: 8103289 [No Abstract] [Full Text] [Related]
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20. Delineation of genetic predisposition to multifactorial disease: a general approach on the threshold of feasibility. Sobell JL; Heston LL; Sommer SS Genomics; 1992 Jan; 12(1):1-6. PubMed ID: 1733846 [No Abstract] [Full Text] [Related] [Next] [New Search]