150 related articles for article (PubMed ID: 8188260)
21. Human alpha-1,3 fucosyltransferase (FucT-VI) gene is located at only 13 kb 3' to the Lewis type fucosyltransferase (FucT-III) gene on chromosome 19.
Nishihara S; Nakazato M; Kudo T; Kimura H; Ando T; Narimatsu H
Biochem Biophys Res Commun; 1993 Jan; 190(1):42-6. PubMed ID: 7916594
[TBL] [Abstract][Full Text] [Related]
22. Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.
Lindsay S; Curtis AR; Roustan P; Kamakari S; Thiselton DL; Stephenson A; Bhattacharya SS
Genomics; 1993 Jul; 17(1):208-10. PubMed ID: 8406451
[TBL] [Abstract][Full Text] [Related]
23. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
Rouquier S; Giorgi D; Trask B; Bergmann A; Phillips MS; MacLennan DH; de Jong P
Genomics; 1993 Aug; 17(2):330-40. PubMed ID: 8406483
[TBL] [Abstract][Full Text] [Related]
24. Defining the proximal border of the Huntington disease candidate region by multipoint recombination analyses.
Skraastad MI; de Rooij KE; de Koning Gans PA; Verwest A; Vegter-van der Vlis M; Bakker E; den Dunnen JT; van Ommen GB
Genomics; 1993 Jun; 16(3):599-604. PubMed ID: 8325632
[TBL] [Abstract][Full Text] [Related]
25. Mapping of 28 (CA)n microsatellite repeats and 13 Alu markers on human chromosome 11 using a panel of somatic cell hybrids.
Iizuka M; Jones C; Hayashi K; Sekiya T
Genomics; 1994 Feb; 19(3):581-4. PubMed ID: 8188304
[No Abstract] [Full Text] [Related]
26. Construction and screening of a cosmid library generated from a somatic cell hybrid bearing human chromosome 15.
McDaniel LD; Zhang B; Kubiczek E; Ritter M; Huang J; Berard C; Leana-Cox J; Schwartz S; Schultz RA
Genomics; 1997 Feb; 40(1):63-72. PubMed ID: 9070920
[TBL] [Abstract][Full Text] [Related]
27. A highly polymorphic locus very tightly linked to the Huntington's disease gene.
Wasmuth JJ; Hewitt J; Smith B; Allard D; Haines JL; Skarecky D; Partlow E; Hayden MR
Nature; 1988 Apr; 332(6166):734-6. PubMed ID: 2895895
[TBL] [Abstract][Full Text] [Related]
28. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.
Haas M; Aburatani H; Stanton VP; Bhatt M; Housman D; Ward DC
Genomics; 1993 Apr; 16(1):90-6. PubMed ID: 8486389
[TBL] [Abstract][Full Text] [Related]
29. The characterization and sequence analysis of thirty CTG-repeat containing genomic cosmid clones.
Philibert RA; Horelli-Kuitunen N; Robb AS; Lee YH; Long RT; Damschroder-Williams P; Martin BM; Brennan MB; Palotie A; Ginns EI
Eur J Hum Genet; 1998 Jan; 6(1):89-94. PubMed ID: 9781019
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Localization of the gene for ATP citrate lyase (ACLY) distal to gastrin(GAS) and proximal to D17S856 on chromosome 17q12-q21.
Couch FJ; Abel KJ; Brody LC; Boehnke M; Collins FS; Weber BL
Genomics; 1994 May; 21(2):444-6. PubMed ID: 8088842
[TBL] [Abstract][Full Text] [Related]
32. A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1).
Kioschis P; Rogner UC; Pick E; Klauck SM; Heiss N; Siebenhaar R; Korn B; Coy JF; Laporte J; Liechti-Gallati S; Poustka A
Genomics; 1996 May; 33(3):365-73. PubMed ID: 8660996
[TBL] [Abstract][Full Text] [Related]
33. The Booroola fecundity (FecB) gene maps to sheep chromosome 6.
Montgomery GW; Lord EA; Penty JM; Dodds KG; Broad TE; Cambridge L; Sunden SL; Stone RT; Crawford AM
Genomics; 1994 Jul; 22(1):148-53. PubMed ID: 7959761
[TBL] [Abstract][Full Text] [Related]
34. Isolation and mapping of 45 NotI linking clones to chromosome 22.
Sanson M; Zhang F; Demczuk S; Delattre O; DeJong P; Aurias A; Thomas G; Rouleau GA
Genomics; 1993 Sep; 17(3):776-9. PubMed ID: 8244398
[TBL] [Abstract][Full Text] [Related]
35. Recombination of 4p16 DNA markers in an unusual family with Huntington disease.
Pritchard C; Zhu N; Zuo J; Bull L; Pericak-Vance MA; Vance JM; Roses AD; Milatovich A; Francke U; Cox DR
Am J Hum Genet; 1992 Jun; 50(6):1218-30. PubMed ID: 1350884
[TBL] [Abstract][Full Text] [Related]
36. The XRCC2 DNA repair gene: identification of a positional candidate.
Tambini CE; George AM; Rommens JM; Tsui LC; Scherer SW; Thacker J
Genomics; 1997 Apr; 41(1):84-92. PubMed ID: 9126486
[TBL] [Abstract][Full Text] [Related]
37. Increased recombination adjacent to the Huntington disease-linked D4S10 marker.
Allitto BA; MacDonald ME; Bucan M; Richards J; Romano D; Whaley WL; Falcone B; Ianazzi J; Wexler NS; Wasmuth JJ
Genomics; 1991 Jan; 9(1):104-12. PubMed ID: 1672283
[TBL] [Abstract][Full Text] [Related]
38. Genomic organization, amplification, fine mapping, and intragenic polymorphisms of the human hemidesmosomal tetraspanin CD151 gene.
Whittock NV; McLean WH
Biochem Biophys Res Commun; 2001 Feb; 281(2):425-30. PubMed ID: 11181065
[TBL] [Abstract][Full Text] [Related]
39. Assignment of the human gene for the beta subunit of the voltage-dependent calcium channel (CACNLB1) to chromosome 17 using somatic cell hybrids and linkage mapping.
Gregg RG; Powers PA; Hogan K
Genomics; 1993 Jan; 15(1):185-7. PubMed ID: 8381767
[TBL] [Abstract][Full Text] [Related]
40. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
De Baere E; Van Roy N; Speleman F; Fukushima Y; De Paepe A; Messiaen L
Genomics; 1999 Apr; 57(1):70-8. PubMed ID: 10191085
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
