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2. Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3. McCombie WR; Martin-Gallardo A; Gocayne JD; FitzGerald M; Dubnick M; Kelley JM; Castilla L; Liu LI; Wallace S; Trapp S Nat Genet; 1992 Aug; 1(5):348-53. PubMed ID: 1338771 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Cloning of the human dopamine D5 receptor gene and identification of a highly polymorphic microsatellite for the DRD5 locus that shows tight linkage to the chromosome 4p reference marker RAF1P1. Sherrington R; Mankoo B; Attwood J; Kalsi G; Curtis D; Buetow K; Povey S; Gurling H Genomics; 1993 Nov; 18(2):423-5. PubMed ID: 8288248 [TBL] [Abstract][Full Text] [Related]
5. Non-random association between DNA markers and Huntington disease locus in the Italian population. Novelletto A; Mandich P; Bellone E; Malaspina P; Vivona G; Ajmar F; Frontali M Am J Med Genet; 1991 Sep; 40(3):374-6. PubMed ID: 1683157 [TBL] [Abstract][Full Text] [Related]
6. Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease. Goldberg YP; Rommens JM; Andrew SE; Hutchinson GB; Lin B; Theilmann J; Graham R; Glaves ML; Starr E; McDonald H Nature; 1993 Mar; 362(6418):370-3. PubMed ID: 8384324 [TBL] [Abstract][Full Text] [Related]
7. Characterization of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISH. Montgomery KT; LeBlanc JM; Tsai P; McNinch JS; Ward DC; de Jong PJ; Kucherlapati R; Krauter KS Genomics; 1993 Sep; 17(3):682-93. PubMed ID: 8244385 [TBL] [Abstract][Full Text] [Related]
8. Frequency and polymorphism of simple sequence repeats in a contiguous 685-kb DNA sequence containing the human T-cell receptor beta-chain gene complex. Charmley P; Concannon P; Hood L; Rowen L Genomics; 1995 Oct; 29(3):760-5. PubMed ID: 8575771 [TBL] [Abstract][Full Text] [Related]
9. A novel tandem repeat sequence located on human chromosome 4p: isolation and characterization. Kogi M; Fukushige S; Lefevre C; Hadano S; Ikeda JE Genomics; 1997 Jun; 42(2):278-83. PubMed ID: 9192848 [TBL] [Abstract][Full Text] [Related]
10. (CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16. Riess O; Weber B; Hayden MR Hum Mol Genet; 1992 Sep; 1(6):452. PubMed ID: 1338762 [No Abstract] [Full Text] [Related]
11. Cloning and mapping of the alpha-adducin gene close to D4S95 and assessment of its relationship to Huntington disease. Goldberg YP; Lin BY; Andrew SE; Nasir J; Graham R; Glaves ML; Hutchinson G; Theilmann J; Ginzinger DG; Schappert K Hum Mol Genet; 1992 Dec; 1(9):669-75. PubMed ID: 1284592 [TBL] [Abstract][Full Text] [Related]
12. Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease. Weber B; Riess O; Wolff G; Andrew S; Collins C; Graham R; Theilmann J; Hayden MR Nat Genet; 1992 Nov; 2(3):216-22. PubMed ID: 1345172 [TBL] [Abstract][Full Text] [Related]
13. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO. Griffith AJ; Burgess DL; Kohrman DC; Yu J; Blaschak J; Blanton SH; Boehnke M; Hecht JT; Overhauser J; Meisler MH Genomics; 1996 Jun; 34(3):299-303. PubMed ID: 8786128 [TBL] [Abstract][Full Text] [Related]
14. Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis. Dodé C; Dürr A; Pêcheux C; Mouret JF; Belal S; Bachner L; Agid Y; Kaplan JC; Brice A; Feingold J C R Acad Sci III; 1993 Nov; 316(11):1374-80. PubMed ID: 8087617 [TBL] [Abstract][Full Text] [Related]
15. Further evidence for clustering of human GABAA receptor subunit genes: localization of the alpha 6-subunit gene (GABRA6) to distal chromosome 5q by linkage analysis. Hicks AA; Bailey ME; Riley BP; Kamphuis W; Siciliano MJ; Johnson KJ; Darlison MG Genomics; 1994 Mar; 20(2):285-8. PubMed ID: 8020978 [TBL] [Abstract][Full Text] [Related]
16. Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively. Collins C; Duff C; Duncan AM; Planells-Cases R; Sun W; Norremolle A; Michaelis E; Montal M; Worton R; Hayden MR Genomics; 1993 Jul; 17(1):237-9. PubMed ID: 8406459 [TBL] [Abstract][Full Text] [Related]
17. Mapping of cosmid clones in Huntington's disease region of chromosome 4. Whaley WL; Bates GP; Novelletto A; Sedlacek Z; Cheng S; Romano D; Ormondroyd E; Allitto B; Lin C; Youngman S Somat Cell Mol Genet; 1991 Jan; 17(1):83-91. PubMed ID: 1671801 [TBL] [Abstract][Full Text] [Related]
18. Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3. Andrew S; Theilmann J; Hedrick A; Mah D; Weber B; Hayden MR Genomics; 1992 Jun; 13(2):301-11. PubMed ID: 1351866 [TBL] [Abstract][Full Text] [Related]
19. A 370-kb cosmid contig of the serpin gene cluster on human chromosome 14q32.1: molecular linkage of the genes encoding alpha 1-antichymotrypsin, protein C inhibitor, kallistatin, alpha 1-antitrypsin, and corticosteroid-binding globulin. Rollini P; Fournier RE Genomics; 1997 Dec; 46(3):409-15. PubMed ID: 9441744 [TBL] [Abstract][Full Text] [Related]
20. [Molecular genetics of Huntington's disease]. Goto J; Masuda N; Watanabe M; Kanazawa I Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]