84 related articles for article (PubMed ID: 8325642)
1. A genetic analysis of the Werner syndrome region on human chromosome 8p.
Thomas W; Rubenstein M; Goto M; Drayna D
Genomics; 1993 Jun; 16(3):685-90. PubMed ID: 8325642
[TBL] [Abstract][Full Text] [Related]
2. Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping.
Ye L; Nakura J; Mitsuda N; Fujioka Y; Kamino K; Ohta T; Jinno Y; Niikawa N; Miki T; Ogihara T
Genomics; 1995 Aug; 28(3):566-9. PubMed ID: 7490095
[TBL] [Abstract][Full Text] [Related]
3. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Yu CE; Oshima J; Hisama FM; Matthews S; Trask BJ; Schellenberg GD
Genomics; 1996 Aug; 35(3):431-40. PubMed ID: 8812476
[TBL] [Abstract][Full Text] [Related]
4. Integrated mapping analysis of the Werner syndrome region of chromosome 8.
Oshima J; Yu CE; Boehnke M; Weber JL; Edelhoff S; Wagner MJ; Wells DE; Wood S; Disteche CM; Martin GM
Genomics; 1994 Sep; 23(1):100-13. PubMed ID: 7829057
[TBL] [Abstract][Full Text] [Related]
5. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.
Todd S; Sherman SL; Naylor SL
Genomics; 1993 Jun; 16(3):612-8. PubMed ID: 8100800
[TBL] [Abstract][Full Text] [Related]
6. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.
Kihara K; Nakura J; Ye L; Mitsuda N; Kamino K; Zhao Y; Fujioka Y; Miki T; Ogihara T
Jpn J Hum Genet; 1994 Dec; 39(4):403-9. PubMed ID: 7873752
[TBL] [Abstract][Full Text] [Related]
7. Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8.
Nakura J; Miki T; Nagano K; Kihara K; Ye L; Kamino K; Fujiwara Y; Yoshida S; Murano S; Fukuchi K
Gerontology; 1993; 39 Suppl 1():11-5. PubMed ID: 8365666
[TBL] [Abstract][Full Text] [Related]
8. Homozygosity mapping of the Werner syndrome locus (WRN).
Nakura J; Wijsman EM; Miki T; Kamino K; Yu CE; Oshima J; Fukuchi K; Weber JL; Piussan C; Melaragno MI
Genomics; 1994 Oct; 23(3):600-8. PubMed ID: 7851888
[TBL] [Abstract][Full Text] [Related]
9. Genetic linkage of Werner's syndrome to five markers on chromosome 8.
Goto M; Rubenstein M; Weber J; Woods K; Drayna D
Nature; 1992 Feb; 355(6362):735-8. PubMed ID: 1741060
[TBL] [Abstract][Full Text] [Related]
10. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
Bateman JB; Geyer DD; Flodman P; Johannes M; Sikela J; Walter N; Moreira AT; Clancy K; Spence MA
Invest Ophthalmol Vis Sci; 2000 Oct; 41(11):3278-85. PubMed ID: 11006214
[TBL] [Abstract][Full Text] [Related]
11. Identification of mutations in DNA polymerase beta mRNAs from patients with Werner syndrome.
Sadakane Y; Maeda K; Kuroda Y; Hori K
Biochem Biophys Res Commun; 1994 Apr; 200(1):219-25. PubMed ID: 7545922
[TBL] [Abstract][Full Text] [Related]
12. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.
Murray JC; Bennett SR; Kwitek AE; Small KW; Schinzel A; Alward WL; Weber JL; Bell GI; Buetow KH
Nat Genet; 1992 Sep; 2(1):46-9. PubMed ID: 1303248
[TBL] [Abstract][Full Text] [Related]
13. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
Vieira H; Gregory-Evans K; Lim N; Brookes JL; Brueton LA; Gregory-Evans CY
Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
[TBL] [Abstract][Full Text] [Related]
14. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
Tsukurov O; Boehmer A; Flynn J; Nicolai JP; Hamel BC; Traill S; Zaleske D; Mankin HJ; Yeon H; Ho C
Nat Genet; 1994 Mar; 6(3):282-6. PubMed ID: 8012391
[TBL] [Abstract][Full Text] [Related]
15. A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
Bateman JB; Richter L; Flodman P; Burch D; Brown S; Penrose P; Paul O; Geyer DD; Brooks DG; Spence MA
Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3441-9. PubMed ID: 16877414
[TBL] [Abstract][Full Text] [Related]
16. Excess of rare cancers in Werner syndrome (adult progeria).
Goto M; Miller RW; Ishikawa Y; Sugano H
Cancer Epidemiol Biomarkers Prev; 1996 Apr; 5(4):239-46. PubMed ID: 8722214
[TBL] [Abstract][Full Text] [Related]
17. A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus.
Bruskiewich R; Schertzer M; Wood S
Genome; 1997 Feb; 40(1):77-83. PubMed ID: 9061915
[TBL] [Abstract][Full Text] [Related]
18. A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference.
Zahn LM; Kwiatkowski DJ
Genomics; 1995 Jul; 28(2):140-6. PubMed ID: 8530019
[TBL] [Abstract][Full Text] [Related]
19. Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.
Melis R; Bradley P; Elsner T; Robertson M; Lawrence E; Gerken S; Albertsen H; White R
Genomics; 1993 Apr; 16(1):56-62. PubMed ID: 8486385
[TBL] [Abstract][Full Text] [Related]
20. A high-resolution linkage map of human 9q34.1.
Henske EP; Ozelius L; Gusella JF; Haines JL; Kwiatkowski DJ
Genomics; 1993 Sep; 17(3):587-91. PubMed ID: 8244374
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
