131 related articles for article (PubMed ID: 1478676)
1. A gene for Usher syndrome type I (USH1A) maps to chromosome 14q.
Kaplan J; Gerber S; Bonneau D; Rozet JM; Delrieu O; Briard ML; Dollfus H; Ghazi I; Dufier JL; Frézal J
Genomics; 1992 Dec; 14(4):979-87. PubMed ID: 1478676
[TBL] [Abstract][Full Text] [Related]
2. Genetic heterogeneity of Usher syndrome type 1 in French families.
Larget-Piet D; Gerber S; Bonneau D; Rozet JM; Marc S; Ghazi I; Dufier JL; David A; Bitoun P; Weissenbach J
Genomics; 1994 May; 21(1):138-43. PubMed ID: 8088781
[TBL] [Abstract][Full Text] [Related]
3. Localization of two genes for Usher syndrome type I to chromosome 11.
Smith RJ; Lee EC; Kimberling WJ; Daiger SP; Pelias MZ; Keats BJ; Jay M; Bird A; Reardon W; Guest M
Genomics; 1992 Dec; 14(4):995-1002. PubMed ID: 1478678
[TBL] [Abstract][Full Text] [Related]
4. Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.
Kimberling WJ; Möller CG; Davenport S; Priluck IA; Beighton PH; Greenberg J; Reardon W; Weston MD; Kenyon JB; Grunkemeyer JA
Genomics; 1992 Dec; 14(4):988-94. PubMed ID: 1478677
[TBL] [Abstract][Full Text] [Related]
5. Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.
Lewis RA; Otterud B; Stauffer D; Lalouel JM; Leppert M
Genomics; 1990 Jun; 7(2):250-6. PubMed ID: 1971808
[TBL] [Abstract][Full Text] [Related]
6. Genetic heterogeneity of Usher syndrome type II in a Dutch population.
Pieke-Dahl S; van Aarem A; Dobin A; Cremers CW; Kimberling WJ
J Med Genet; 1996 Sep; 33(9):753-7. PubMed ID: 8880575
[TBL] [Abstract][Full Text] [Related]
7. Localization of Usher syndrome type II to chromosome 1q.
Kimberling WJ; Weston MD; Möller C; Davenport SL; Shugart YY; Priluck IA; Martini A; Milani M; Smith RJ
Genomics; 1990 Jun; 7(2):245-9. PubMed ID: 2347588
[TBL] [Abstract][Full Text] [Related]
8. Evidence for a fourth locus in Usher syndrome type I.
Gerber S; Larget-Piet D; Rozet JM; Bonneau D; Mathieu M; Der Kaloustian V; Munnich A; Kaplan J
J Med Genet; 1996 Jan; 33(1):77-9. PubMed ID: 8825055
[TBL] [Abstract][Full Text] [Related]
9. A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21.
Chaïb H; Kaplan J; Gerber S; Vincent C; Ayadi H; Slim R; Munnich A; Weissenbach J; Petit C
Hum Mol Genet; 1997 Jan; 6(1):27-31. PubMed ID: 9002666
[TBL] [Abstract][Full Text] [Related]
10. Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.
Humphries P; Farrar GJ; Kenna P; McWilliam P
Clin Genet; 1990 Jul; 38(1):1-13. PubMed ID: 2201466
[TBL] [Abstract][Full Text] [Related]
11. Linkage analysis in Usher syndrome type I (USH1) families from Spain.
Espinós C; Nájera C; Millán JM; Ayuso C; Baiget M; Pérez-Garrigues H; Rodrigo O; Vilela C; Beneyto M
J Med Genet; 1998 May; 35(5):391-8. PubMed ID: 9610802
[TBL] [Abstract][Full Text] [Related]
12. Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
Astuto LM; Weston MD; Carney CA; Hoover DM; Cremers CW; Wagenaar M; Moller C; Smith RJ; Pieke-Dahl S; Greenberg J; Ramesar R; Jacobson SG; Ayuso C; Heckenlively JR; Tamayo M; Gorin MB; Reardon W; Kimberling WJ
Am J Hum Genet; 2000 Dec; 67(6):1569-74. PubMed ID: 11060213
[TBL] [Abstract][Full Text] [Related]
13. Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium.
Keats BJ; Todorov AA; Atwood LD; Pelias MZ; Hejtmancik JF; Kimberling WJ; Leppert M; Lewis RA; Smith RJ
Genomics; 1992 Nov; 14(3):707-14. PubMed ID: 1427898
[TBL] [Abstract][Full Text] [Related]
14. Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.
Pieke-Dahl S; Möller CG; Kelley PM; Astuto LM; Cremers CW; Gorin MB; Kimberling WJ
J Med Genet; 2000 Apr; 37(4):256-62. PubMed ID: 10745043
[TBL] [Abstract][Full Text] [Related]
15. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
Hmani M; Ghorbel A; Boulila-Elgaied A; Ben Zina Z; Kammoun W; Drira M; Chaabouni M; Petit C; Ayadi H
Eur J Hum Genet; 1999 Apr; 7(3):363-7. PubMed ID: 10234513
[TBL] [Abstract][Full Text] [Related]
16. The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region.
Saouda M; Mansour A; Bou Moglabey Y; El Zir E; Mustapha M; Chaib H; Nehmé A; Mégarbané A; Loiselet J; Petit C; Slim R
Hum Genet; 1998 Aug; 103(2):193-8. PubMed ID: 9760205
[TBL] [Abstract][Full Text] [Related]
17. Genetic heterogeneity of Usher syndrome type II.
Pieke Dahl S; Kimberling WJ; Gorin MB; Weston MD; Furman JM; Pikus A; Möller C
J Med Genet; 1993 Oct; 30(10):843-8. PubMed ID: 7901420
[TBL] [Abstract][Full Text] [Related]
18. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
Mustapha M; Chouery E; Torchard-Pagnez D; Nouaille S; Khrais A; Sayegh FN; Mégarbané A; Loiselet J; Lathrop M; Petit C; Weil D
Hum Genet; 2002 Apr; 110(4):348-50. PubMed ID: 11941484
[TBL] [Abstract][Full Text] [Related]
19. Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.
Keats BJ; Nouri N; Pelias MZ; Deininger PL; Litt M
Am J Hum Genet; 1994 Apr; 54(4):681-6. PubMed ID: 8128966
[TBL] [Abstract][Full Text] [Related]
20. A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p.
Papaioannou M; Chakarova CF; Prescott DC; Waseem N; Theis T; Lopez I; Gill B; Koenekoop RK; Bhattacharya SS
Hum Genet; 2005 Dec; 118(3-4):501-3. PubMed ID: 16189705
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
