110 related articles for article (PubMed ID: 2288459)
1. Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneity.
Kaplan J; Guasconi G; Dufier JL; Michel-Awad A; David A; Munnich A; Frezal J
Ann Genet; 1990; 33(3):152-4. PubMed ID: 2288459
[TBL] [Abstract][Full Text] [Related]
2. Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneity.
Kaplan J; Guasconi G; Bonneau D; Melki J; Briard ML; Munnich A; Dufier JL; Frézal J
Ann Genet; 1990; 33(2):105-8. PubMed ID: 1978628
[TBL] [Abstract][Full Text] [Related]
3. Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.
Olsson JE; Samanns C; Jimenez J; Pongratz J; Chand A; Watty A; Seuchter SA; Denton M; Gal A
Am J Med Genet; 1990 Apr; 35(4):595-9. PubMed ID: 2333895
[TBL] [Abstract][Full Text] [Related]
4. Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.
Blanton SH; Cottingham AW; Giesenschlag N; Heckenlively JR; Humphries P; Daiger SP
Genomics; 1990 Sep; 8(1):179-81. PubMed ID: 2081594
[TBL] [Abstract][Full Text] [Related]
5. No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity.
Inglehearn CF; Jay M; Lester DH; Bashir R; Jay B; Bird AC; Wright AF; Evans HJ; Papiha SS; Bhattacharya SS
Genomics; 1990 Jan; 6(1):168-73. PubMed ID: 2303257
[TBL] [Abstract][Full Text] [Related]
6. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
Benomar A; Le Guern E; Dürr A; Ouhabi H; Stevanin G; Yahyaoui M; Chkili T; Agid Y; Brice A
Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871
[TBL] [Abstract][Full Text] [Related]
7. Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families.
Inglehearn CF; Lester DH; Bashir R; Atif U; Keen TJ; Sertedaki A; Lindsey J; Jay M; Bird AC; Farrar GJ
Am J Hum Genet; 1992 Mar; 50(3):590-7. PubMed ID: 1539595
[TBL] [Abstract][Full Text] [Related]
8. No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian families.
Jiménez JB; Samanns C; Watty A; Pongratz J; Olsson JE; Dickinson P; Buttery R; Gal A; Denton MJ
Hum Genet; 1991 Jan; 86(3):265-7. PubMed ID: 1997379
[TBL] [Abstract][Full Text] [Related]
9. Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.
Jordan SA; Farrar GJ; Kenna P; Humphries MM; Sheils DM; Kumar-Singh R; Sharp EM; Soriano N; Ayuso C; Benitez J
Nat Genet; 1993 May; 4(1):54-8. PubMed ID: 8513324
[TBL] [Abstract][Full Text] [Related]
10. [A study on localization of an autosomal dominant retinitis pigmentosa gene].
Ma X; Wei R; Cai J; Zhu L
Zhonghua Yan Ke Za Zhi; 2002 Nov; 38(11):680-3. PubMed ID: 12487900
[TBL] [Abstract][Full Text] [Related]
11. Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.
Lester DH; Inglehearn CF; Bashir R; Ackford H; Esakowitz L; Jay M; Bird AC; Wright AF; Papiha SS; Bhattacharya SS
Am J Hum Genet; 1990 Sep; 47(3):536-41. PubMed ID: 2393026
[TBL] [Abstract][Full Text] [Related]
12. Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin.
Greenberg J; Babaya M; Ramesar R; Beighton P
Clin Genet; 1992 Jun; 41(6):322-5. PubMed ID: 1623630
[TBL] [Abstract][Full Text] [Related]
13. Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosa.
Kumar-Singh R; Kenna PF; Farrar GJ; Humphries P
Genomics; 1993 Jan; 15(1):212-5. PubMed ID: 8432539
[TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Ahmad Z; Riazuddin S; Hejtmancik JF
Mol Vis; 2004 Nov; 10():884-9. PubMed ID: 15570217
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
McWilliam P; Farrar GJ; Kenna P; Bradley DG; Humphries MM; Sharp EM; McConnell DJ; Lawler M; Sheils D; Ryan C
Genomics; 1989 Oct; 5(3):619-22. PubMed ID: 2613244
[TBL] [Abstract][Full Text] [Related]
17. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
Riazuddin SA; Zulfiqar F; Zhang Q; Sergeev YV; Qazi ZA; Husnain T; Caruso R; Riazuddin S; Sieving PA; Hejtmancik JF
Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
[TBL] [Abstract][Full Text] [Related]
19. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
Ayuso C; Garcia-Sandoval B; Najera C; Valverde D; Carballo M; Antiñolo G
Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
[TBL] [Abstract][Full Text] [Related]
20. Epidemiology of retinitis pigmentosa in the Valencian community (Spain).
Nájera C; Millán JM; Beneyto M; Prieto F
Genet Epidemiol; 1995; 12(1):37-46. PubMed ID: 7713399
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]