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.
76 related articles for article (PubMed ID: 7800703)
1. Linkage analysis: progress and problems. Bishop DT Philos Trans R Soc Lond B Biol Sci; 1994 Jun; 344(1310):337-43. PubMed ID: 7800703 [TBL] [Abstract][Full Text] [Related]
2. Genetic analysis workshop 9: development of problem 1. Hodge SE Genet Epidemiol; 1995; 12(6):555-60. PubMed ID: 8787972 [TBL] [Abstract][Full Text] [Related]
3. The genealogic approach to human genetics of disease. Gulcher J; Kong A; Stefansson K Cancer J; 2001; 7(1):61-8. PubMed ID: 11269649 [TBL] [Abstract][Full Text] [Related]
4. An oliogenic disease displaying weak marker associations: a summary of contributions to problem 1 of GAW9. Hodge SE Genet Epidemiol; 1995; 12(6):545-54. PubMed ID: 8787971 [TBL] [Abstract][Full Text] [Related]
5. Molecular genetic approaches to the study of individual risk in alcoholism. Worton RG Alcohol Alcohol Suppl; 1991; 1():19-25. PubMed ID: 1845536 [TBL] [Abstract][Full Text] [Related]
6. Linkage and association. Morton NE Prog Clin Biol Res; 1984; 147():245-65. PubMed ID: 6377314 [No Abstract] [Full Text] [Related]
7. A general method for linkage disequilibrium correction for multipoint linkage and association. Kurbasic A; Hössjer O Genet Epidemiol; 2008 Nov; 32(7):647-57. PubMed ID: 18481794 [TBL] [Abstract][Full Text] [Related]
8. The use of a genetic map of biallelic markers in linkage studies. Kruglyak L Nat Genet; 1997 Sep; 17(1):21-4. PubMed ID: 9288093 [TBL] [Abstract][Full Text] [Related]
9. LINKAGE programs: linkage analysis for monogenic cardiovascular diseases. Li L; Wang QK; Rao S Methods Mol Med; 2006; 128():41-60. PubMed ID: 17071989 [TBL] [Abstract][Full Text] [Related]
10. Identifying genetic risk factors for osteoporosis. Uitterlinden AG; van Meurs JB; Rivadeneira F; Pols HA J Musculoskelet Neuronal Interact; 2006; 6(1):16-26. PubMed ID: 16675886 [TBL] [Abstract][Full Text] [Related]
11. Mapping disease genes using the Malecot model for allelic association and the beta model for linkage. Collins A Clin Exp Allergy; 1999 Dec; 29 Suppl 4():53-6. PubMed ID: 10641568 [TBL] [Abstract][Full Text] [Related]
12. Population choice in mapping genes for complex diseases. Wright AF; Carothers AD; Pirastu M Nat Genet; 1999 Dec; 23(4):397-404. PubMed ID: 10581024 [TBL] [Abstract][Full Text] [Related]
13. Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency. Indo Y; Mardy S; Miura Y; Moosa A; Ismail EA; Toscano E; Andria G; Pavone V; Brown DL; Brooks A; Endo F; Matsuda I Hum Mutat; 2001 Oct; 18(4):308-18. PubMed ID: 11668614 [TBL] [Abstract][Full Text] [Related]
14. Two-locus approach of segregation and linkage analysis in the study of complex traits. Xu J; Taylor EW; Panhuysen CI; Prenger VL; Koskela R; Kiemeney B; LaBuda MC; Maestri NE; Meyers DA Genet Epidemiol; 1995; 12(6):825-30. PubMed ID: 8788016 [TBL] [Abstract][Full Text] [Related]
15. An efficient, robust and unified method for mapping complex traits (III): combined linkage/linkage-disequilibrium analysis. Zhao LP; Quiaoit F; Aragaki C; Hsu L Am J Med Genet; 1999 Jun; 84(5):433-53. PubMed ID: 10360398 [TBL] [Abstract][Full Text] [Related]
16. Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia. Arolt V; Lencer R; Purmann S; Schürmann M; Müller-Myhsok B; Krecker K; Schwinger E Am J Med Genet; 1999 Dec; 88(6):603-6. PubMed ID: 10581476 [No Abstract] [Full Text] [Related]