198 related articles for article (PubMed ID: 17211611)
21. Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.
de Brouwer AP; Kunst HP; Krebsova A; van Asseldonk K; Reis A; Snoeckx RL; Van Camp G; Cremers CW; Cremers FP; Kremer H
Am J Med Genet A; 2005 Aug; 137(1):41-6. PubMed ID: 16007628
[TBL] [Abstract][Full Text] [Related]
22. DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.
Basit S; Lee K; Habib R; Chen L; Umm-e-Kalsoom ; Santos-Cortez RL; Azeem Z; Andrade P; Ansar M; Ahmad W; Leal SM
Hum Genet; 2011 Apr; 129(4):379-85. PubMed ID: 21181198
[TBL] [Abstract][Full Text] [Related]
23. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
Ansar M; Ramzan M; Pham TL; Yan K; Jamal SM; Haque S; Ahmad W; Leal SM
Hum Hered; 2003; 55(1):71-4. PubMed ID: 12890929
[TBL] [Abstract][Full Text] [Related]
24. Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.
Viollet L; Zarhrate M; Maystadt I; Estournet-Mathiaut B; Barois A; Desguerre I; Mayer M; Chabrol B; LeHeup B; Cusin V; Billette De Villemeur T; Bonneau D; Saugier-Veber P; Touzery-De Villepin A; Delaubier A; Kaplan J; Jeanpierre M; Feingold J; Munnich A
Eur J Hum Genet; 2004 Jun; 12(6):483-8. PubMed ID: 15054395
[TBL] [Abstract][Full Text] [Related]
25. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Riazuddin S; Nazli S; Ahmed ZM; Yang Y; Zulfiqar F; Shaikh RS; Zafar AU; Khan SN; Sabar F; Javid FT; Wilcox ER; Tsilou E; Boger ET; Sellers JR; Belyantseva IA; Riazuddin S; Friedman TB
Hum Mutat; 2008 Apr; 29(4):502-11. PubMed ID: 18181211
[TBL] [Abstract][Full Text] [Related]
26. Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.
Collin RW; Kalay E; Oostrik J; Caylan R; Wollnik B; Arslan S; den Hollander AI; Birinci Y; Lichtner P; Strom TM; Toraman B; Hoefsloot LH; Cremers CW; Brunner HG; Cremers FP; Karaguzel A; Kremer H
Hum Mutat; 2007 Jul; 28(7):718-23. PubMed ID: 17373699
[TBL] [Abstract][Full Text] [Related]
27. [Gene mapping of a nonsyndromic hearing impairmint family].
Cheng L; Gong Y; Liu Q; Chen B; Guo C; Li J; Zhang X; Lu Y; Gao G; Zhou H; Guo Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):89-93. PubMed ID: 12673573
[TBL] [Abstract][Full Text] [Related]
28. DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22.
Ansar M; Chahrour MH; Amin Ud Din M; Arshad M; Haque S; Pham TL; Yan K; Ahmad W; Leal SM
Hum Hered; 2004; 57(4):195-9. PubMed ID: 15583425
[TBL] [Abstract][Full Text] [Related]
29. A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
Riazuddin SA; Yasmeen A; Zhang Q; Yao W; Sabar MF; Ahmed Z; Riazuddin S; Hejtmancik JF
Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):623-6. PubMed ID: 15671291
[TBL] [Abstract][Full Text] [Related]
30. Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.
Khaliq S; Hameed A; Ismail M; Anwar K; Leroy BP; Mehdi SQ; Payne AM; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):3709-12. PubMed ID: 11053266
[TBL] [Abstract][Full Text] [Related]
31. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.
Mangino M; Flex E; Capon F; Sangiuolo F; Carraro E; Gualandi F; Mazzoli M; Martini A; Novelli G; Dallapiccola B
Eur J Hum Genet; 2001 Sep; 9(9):667-71. PubMed ID: 11571554
[TBL] [Abstract][Full Text] [Related]
32. A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p.
Naz S; Riazuddin SA; Li L; Shahid M; Kousar S; Sieving PA; Hejtmancik JF; Riazuddin S
Am J Ophthalmol; 2010 May; 149(5):861-6. PubMed ID: 20227676
[TBL] [Abstract][Full Text] [Related]
33. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
Wali A; Chishti M; Ayub M; Yasinzai M; Kafaitullah ; Ali G; John P; Ahmad W
Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
[TBL] [Abstract][Full Text] [Related]
34. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
Danciger M; Hendrickson J; Lyon J; Toomes C; McHale JC; Fishman GA; Inglehearn CF; Jacobson SG; Farber DB
Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2458-65. PubMed ID: 11581183
[TBL] [Abstract][Full Text] [Related]
35. [Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment].
Zhu QH; Li H; Liu P; Zhu ZF; Wang X; Yuan WL; Liu JY; Mao HY; Wang Q; Liu MG
Yi Chuan; 2007 Feb; 29(2):172-6. PubMed ID: 17369171
[TBL] [Abstract][Full Text] [Related]
36. Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees.
Katsanis N; Lewis RA; Stockton DW; Mai PM; Baird L; Beales PL; Leppert M; Lupski JR
Am J Hum Genet; 1999 Dec; 65(6):1672-9. PubMed ID: 10577921
[TBL] [Abstract][Full Text] [Related]
37. A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.
Hameed A; Khaliq S; Ismail M; Anwar K; Mehdi SQ; Bessant D; Payne AM; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1436-8. PubMed ID: 11381043
[TBL] [Abstract][Full Text] [Related]
38. A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12.
Chouery E; Kfoury J; Delague V; Jalkh N; Bejjani P; Serre JL; Mégarbané A
Neurogenetics; 2008 Oct; 9(4):287-93. PubMed ID: 18688663
[TBL] [Abstract][Full Text] [Related]
39. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
Hand CK; Harmon DL; Kennedy SM; FitzSimon JS; Collum LM; Parfrey NA
Genomics; 1999 Oct; 61(1):1-4. PubMed ID: 10512674
[TBL] [Abstract][Full Text] [Related]
40. A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus.
Jain PK; Fukushima K; Deshmukh D; Ramesh A; Thomas E; Lalwani AK; Kumar S; Plopis B; Skarka H; Srisailapathy CR
Hum Mol Genet; 1995 Dec; 4(12):2391-4. PubMed ID: 8634715
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
