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84. Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate. Ophoff RA; Escamilla MA; Service SK; Spesny M; Meshi DB; Poon W; Molina J; Fournier E; Gallegos A; Mathews C; Neylan T; Batki SL; Roche E; Ramirez M; Silva S; De Mille MC; Dong P; Leon PE; Reus VI; Sandkuijl LA; Freimer NB Am J Hum Genet; 2002 Sep; 71(3):565-74. PubMed ID: 12119601 [TBL] [Abstract][Full Text] [Related]
85. Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41. Watanabe Y; Murray JC; Bjork BC; Bird CP; Chiang PW; Gregory SG; Kurnit DM; Schutte BC Hum Mutat; 2001 Nov; 18(5):422-34. PubMed ID: 11668635 [TBL] [Abstract][Full Text] [Related]
86. 4p16.3 haplotype modifying age at onset of Huntington disease. Nørremølle A; Budtz-Jørgensen E; Fenger K; Nielsen JE; Sørensen SA; Hasholt L Clin Genet; 2009 Mar; 75(3):244-50. PubMed ID: 19250382 [TBL] [Abstract][Full Text] [Related]
87. A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients. Pritchard C; Casher D; Bull L; Cox DR; Myers RM Proc Natl Acad Sci U S A; 1990 Sep; 87(18):7309-13. PubMed ID: 2144903 [TBL] [Abstract][Full Text] [Related]
88. Origins and evolution of Huntington disease chromosomes. Andrew SE; Hayden MR Neurodegeneration; 1995 Sep; 4(3):239-44. PubMed ID: 8581556 [TBL] [Abstract][Full Text] [Related]
89. A first-generation linkage disequilibrium map of human chromosome 22. Dawson E; Abecasis GR; Bumpstead S; Chen Y; Hunt S; Beare DM; Pabial J; Dibling T; Tinsley E; Kirby S; Carter D; Papaspyridonos M; Livingstone S; Ganske R; Lõhmussaar E; Zernant J; Tõnisson N; Remm M; Mägi R; Puurand T; Vilo J; Kurg A; Rice K; Deloukas P; Mott R; Metspalu A; Bentley DR; Cardon LR; Dunham I Nature; 2002 Aug; 418(6897):544-8. PubMed ID: 12110843 [TBL] [Abstract][Full Text] [Related]
90. Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I population. Peral B; Ward CJ; San Millán JL; Thomas S; Stallings RL; Moreno F; Harris PC Am J Hum Genet; 1994 May; 54(5):899-908. PubMed ID: 7909986 [TBL] [Abstract][Full Text] [Related]
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92. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene. Baxendale S; MacDonald ME; Mott R; Francis F; Lin C; Kirby SF; James M; Zehetner G; Hummerich H; Valdes J Nat Genet; 1993 Jun; 4(2):181-6. PubMed ID: 8348156 [TBL] [Abstract][Full Text] [Related]
93. Allelic association with SNPs: metrics, populations, and the linkage disequilibrium map. Collins A; Ennis S; Taillon-Miller P; Kwok PY; Morton NE Hum Mutat; 2001 Apr; 17(4):255-62. PubMed ID: 11295822 [TBL] [Abstract][Full Text] [Related]
94. The Huntington's disease candidate region exhibits many different haplotypes. MacDonald ME; Novelletto A; Lin C; Tagle D; Barnes G; Bates G; Taylor S; Allitto B; Altherr M; Myers R Nat Genet; 1992 May; 1(2):99-103. PubMed ID: 1302016 [TBL] [Abstract][Full Text] [Related]
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96. Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8). Quarrell OW; Youngman S; Sarfarazi M; Harper PS J Med Genet; 1988 Mar; 25(3):191-4. PubMed ID: 2895189 [TBL] [Abstract][Full Text] [Related]
97. The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD. Farrer LA; Cupples LA; Wiater P; Conneally PM; Gusella JF; Myers RH Am J Hum Genet; 1993 Jul; 53(1):125-30. PubMed ID: 8317477 [TBL] [Abstract][Full Text] [Related]
98. Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3. Lesperance MM; Burmeister M Am J Hum Genet; 2000 Jul; 67(1):262-3. PubMed ID: 10848501 [No Abstract] [Full Text] [Related]
99. Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region. Watkins WS; Zenger R; O'Brien E; Nyman D; Eriksson AW; Renlund M; Jorde LB Am J Hum Genet; 1994 Aug; 55(2):348-55. PubMed ID: 7913583 [TBL] [Abstract][Full Text] [Related]
100. Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q. Litt M; Jorde LB Am J Hum Genet; 1986 Aug; 39(2):166-78. PubMed ID: 3019131 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]