212 related articles for article (PubMed ID: 7902160)
1. Allelic association and linkage studies in Wilson disease.
Thomas GR; Roberts EA; Rosales TO; Moroz SP; Lambert MA; Wong LT; Cox DW
Hum Mol Genet; 1993 Sep; 2(9):1401-5. PubMed ID: 7902160
[TBL] [Abstract][Full Text] [Related]
2. A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus.
White A; Tomfohrde J; Stewart E; Barnes R; Le Paslier D; Weissenbach J; Cavalli-Sforza L; Farrer L; Bowcock A
Proc Natl Acad Sci U S A; 1993 Nov; 90(21):10105-9. PubMed ID: 8234264
[TBL] [Abstract][Full Text] [Related]
3. Long range restriction mapping of 13q14.3 focused on the Wilson disease region.
Bull PC; Cox DW
Genomics; 1993 Jun; 16(3):593-8. PubMed ID: 8325631
[TBL] [Abstract][Full Text] [Related]
4. Polymorphic microsatellites and Wilson disease (WD).
Stewart EA; White A; Tomfohrde J; Osborne-Lawrence S; Prestridge L; Bonne-Tamir B; Scheinberg IH; St George-Hyslop P; Giagheddu M; Kim JW
Am J Hum Genet; 1993 Oct; 53(4):864-73. PubMed ID: 8213814
[TBL] [Abstract][Full Text] [Related]
5. Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene.
Scheffer H; Houwen RH; Te Meerman GJ; Loessner J; Bachmann B; Kunert E; Verlind E; Buys CH
Hum Genet; 1992 Aug; 89(6):607-11. PubMed ID: 1511977
[TBL] [Abstract][Full Text] [Related]
6. Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.
Bowcock AM; Tomfohrde J; Weissenbach J; Bonne-Tamir B; St George-Hyslop P; Giagheddu M; Cavalli-Sforza LL; Farrer LA
Am J Hum Genet; 1994 Jan; 54(1):79-87. PubMed ID: 8279473
[TBL] [Abstract][Full Text] [Related]
7. Haplotype studies in Wilson disease.
Thomas GR; Bull PC; Roberts EA; Walshe JM; Cox DW
Am J Hum Genet; 1994 Jan; 54(1):71-8. PubMed ID: 8279472
[TBL] [Abstract][Full Text] [Related]
8. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
Bowcock AM; Farrer LA; Cavalli-Sforza LL; Hebert JM; Kidd KK; Frydman M; Bonne-Tamir B
Am J Hum Genet; 1987 Jul; 41(1):27-35. PubMed ID: 3474893
[TBL] [Abstract][Full Text] [Related]
9. Eight closely linked loci place the Wilson disease locus within 13q14-q21.
Bowcock AM; Farrer LA; Hebert JM; Agger M; Sternlieb I; Scheinberg IH; Buys CH; Scheffer H; Frydman M; Chajek-Saul T
Am J Hum Genet; 1988 Nov; 43(5):664-74. PubMed ID: 3189332
[TBL] [Abstract][Full Text] [Related]
10. Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.
Haines JL; Ozelius L; St George-Hyslop P; Wexler NS; Gusella JF; Conneally PM
Genet Epidemiol; 1988; 5(6):375-80. PubMed ID: 2905314
[TBL] [Abstract][Full Text] [Related]
11. Predictive testing for Wilson's disease using tightly linked and flanking DNA markers.
Farrer LA; Bowcock AM; Hebert JM; Bonné-Tamir B; Sternlieb I; Giagheddu M; St George-Hyslop P; Frydman M; Lössner J; Demelia L
Neurology; 1991 Jul; 41(7):992-9. PubMed ID: 2067662
[TBL] [Abstract][Full Text] [Related]
12. Close linkage of the Wilson's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14.
Houwen RH; Scheffer H; te Meerman GJ; van der Vlies P; Buys CH
Hum Genet; 1990 Oct; 85(5):560-2. PubMed ID: 2227943
[TBL] [Abstract][Full Text] [Related]
13. Isolation of new probes in the region of the Wilson disease locus, 13q14.2-->q14.3.
Bull PC; Barwell JA; Hannah HT; Pautler SE; Higgins MJ; Lalande M; Cox DW
Cytogenet Cell Genet; 1993; 64(1):12-7. PubMed ID: 8508673
[TBL] [Abstract][Full Text] [Related]
14. Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.
Figus A; Lampis R; Devoto M; Ristaldi MS; Ideo A; de Virgilis S; Nurchi AM; Corrias A; Corda R; Lai ME
J Med Genet; 1989 Feb; 26(2):78-82. PubMed ID: 2563776
[TBL] [Abstract][Full Text] [Related]
15. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.
Petrukhin K; Fischer SG; Pirastu M; Tanzi RE; Chernov I; Devoto M; Brzustowicz LM; Cayanis E; Vitale E; Russo JJ
Nat Genet; 1993 Dec; 5(4):338-43. PubMed ID: 8298640
[TBL] [Abstract][Full Text] [Related]
16. Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13.
Kooy RF; Van der Veen AY; Verlind E; Houwen RH; Scheffer H; Buys CH
Hum Genet; 1993 Jun; 91(5):504-6. PubMed ID: 8314565
[TBL] [Abstract][Full Text] [Related]
17. A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in 10 intervals.
Kooy RF; Verlind E; Houwen RH; Shapiro DN; Hawthorn LA; Cowell JK; Scheffer H; Buys CH
Eur J Hum Genet; 1994; 2(1):59-65. PubMed ID: 7913868
[TBL] [Abstract][Full Text] [Related]
18. DNA markers for the diagnosis of Wilson disease.
Houwen RH; Roberts EA; Thomas GR; Cox DW
J Hepatol; 1993 Mar; 17(3):269-76. PubMed ID: 8100247
[TBL] [Abstract][Full Text] [Related]
19. Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.
Farrer LA; Bonne-Tamir B; Frydman M; Magazanik A; Kidd KK; Bowcock AM; Cavalli-Sforza LL
Hum Genet; 1988 Jun; 79(2):109-17. PubMed ID: 3164701
[TBL] [Abstract][Full Text] [Related]
20. Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan.
Chuang LM; Tai TY; Wang TR; Chang YC; Chen KH; Lin RS; Lin BJ
Hum Genet; 1991 Aug; 87(4):465-8. PubMed ID: 1679032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]