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Results: 1 to 20 of 158

Similar articles for PubMed (Select 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.

PMID:
8325642
2.

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, et al.

Genomics. 1994 Sep 1;23(1):100-13.

PMID:
7829057
3.

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, et al.

Gerontology. 1993;39 Suppl 1:11-5.

PMID:
8365666
4.

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, et al.

Genomics. 1994 Oct;23(3):600-8.

PMID:
7851888
5.

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 10;28(3):566-9.

PMID:
7490095
6.

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.

PMID:
9061915
7.

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, Friedman LH, Daiger SP.

Genomics. 1991 Dec;11(4):857-69.

PMID:
1783394
8.

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 1;35(3):431-40.

PMID:
8812476
9.

Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22.

Nagano K, Nakura J, Kihara K, Ye L, Kamino K, Mitsuda N, Ohta T, Jinno Y, Niikawa N, Miki T, et al.

Jpn J Hum Genet. 1993 Dec;38(4):391-7.

PMID:
8186416
10.
11.

A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8.

Chaffanet M, Imbert A, Adélaïde J, Le Paslier D, Wagner MJ, Wells DE, Birnbaum D, Pébusque MJ.

Cytogenet Cell Genet. 1996;72(1):63-8.

PMID:
8565638
12.

Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome.

Imbert A, Chaffanet M, Essioux L, Noguchi T, Adélaïde J, Kerangueven F, Le Paslier D, Bonaïti-Pellié C, Sobol H, Birnbaum D, Pébusque MJ.

Genomics. 1996 Feb 15;32(1):29-38.

PMID:
8786118
13.

Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

Yu CE, Oshima J, Goddard KA, Miki T, Nakura J, Ogihara T, Poot M, Hoehn H, Fraccaro M, Piussan C, et al.

Am J Hum Genet. 1994 Aug;55(2):356-64.

14.

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Goddard KA, Yu CE, Oshima J, Miki T, Nakura J, Piussan C, Martin GM, Schellenberg GD, Wijsman EM.

Am J Hum Genet. 1996 Jun;58(6):1286-302.

15.

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, Ogihara T.

Genomics. 1996 Aug 15;36(1):130-41.

PMID:
8812424
16.

[Genetic analysis of Werner syndrome in a family].

Morishima A, Mitsuda N, Nakura J, Kamino K, Sato N, Miki T, Ogihara T.

Nihon Ronen Igakkai Zasshi. 1995 Dec;32(12):817-21. Japanese.

17.

Construction of a GT polymorphism map of human 9q.

Kwiatkowski DJ, Henske EP, Weimer K, Ozelius L, Gusella JF, Haines J.

Genomics. 1992 Feb;12(2):229-40.

PMID:
1339384
18.

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.

PMID:
7873752
19.

Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker.

Petersen MB, Economou EP, Slaugenhaupt SA, Chakravarti A, Antonarakis SE.

Genomics. 1990 May;7(1):136-8.

PMID:
1970797
20.

Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.

Petersen MB, Weber JL, Slaugenhaupt SA, Kwitek AE, McInnis MG, Chakravarti A, Antonarakis SE.

Hum Genet. 1991 Aug;87(4):401-4.

PMID:
1879826
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