155 related articles for article (PubMed ID: 10364526)
1. A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.
Fukushima K; Kasai N; Ueki Y; Nishizaki K; Sugata K; Hirakawa S; Masuda A; Gunduz M; Ninomiya Y; Masuda Y; Sato M; McGuirt WT; Coucke P; Van Camp G; Smith RJ
Am J Hum Genet; 1999 Jul; 65(1):141-50. PubMed ID: 10364526
[TBL] [Abstract][Full Text] [Related]
2. Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.
Kasai N; Fukushima K; Ueki Y; Prasad S; Nosakowski J; Sugata K; Sugata A; Nishizaki K; Meyer NC; Smith RJ
Gene; 2001 Feb; 264(1):113-22. PubMed ID: 11245985
[TBL] [Abstract][Full Text] [Related]
3. A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.
Pulleyn LJ; Jackson AP; Roberts E; Carridice A; Muxworthy C; Houseman M; Al-Gazali LI; Lench NJ; Markham AF; Mueller RF
Eur J Hum Genet; 2000 Dec; 8(12):991-3. PubMed ID: 11175289
[TBL] [Abstract][Full Text] [Related]
4. A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.
Chatterjee A; Jalvi R; Pandey N; Rangasayee R; Anand A
Hum Genet; 2009 Jan; 124(6):669-75. PubMed ID: 19030898
[TBL] [Abstract][Full Text] [Related]
5. Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.
Balciuniene J; Dahl N; Borg E; Samuelsson E; Koisti MJ; Pettersson U; Jazin EE
Am J Hum Genet; 1998 Sep; 63(3):786-93. PubMed ID: 9718342
[TBL] [Abstract][Full Text] [Related]
6. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.
Modamio-Høybjør S; Moreno-Pelayo MA; Mencía A; del Castillo I; Chardenoux S; Morais D; Lathrop M; Petit C; Moreno F
J Med Genet; 2004 Feb; 41(2):e14. PubMed ID: 14757864
[No Abstract] [Full Text] [Related]
7. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
Brown MR; Tomek MS; Van Laer L; Smith S; Kenyon JB; Van Camp G; Smith RJ
Am J Hum Genet; 1997 Oct; 61(4):924-7. PubMed ID: 9382104
[TBL] [Abstract][Full Text] [Related]
8. A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
Verhoeven K; Van Camp G; Govaerts PJ; Balemans W; Schatteman I; Verstreken M; Van Laer L; Smith RJ; Brown MR; Van de Heyning PH; Somers T; Offeciers FE; Willems PJ
Am J Hum Genet; 1997 May; 60(5):1168-73. PubMed ID: 9150164
[TBL] [Abstract][Full Text] [Related]
9. Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.
Akita J; Abe S; Shinkawa H; Kimberling WJ; Usami S
J Hum Genet; 2001; 46(7):355-61. PubMed ID: 11450843
[TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.
Prakash S; Chung KW; Sinha S; Barmada M; Ellis D; Ferrell RE; Finegold DN; Randhawa PS; Dinda A; Vats A
J Am Soc Nephrol; 2003 Jul; 14(7):1794-803. PubMed ID: 12819239
[TBL] [Abstract][Full Text] [Related]
11. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
Xia J; Deng H; Feng Y; Zhang H; Pan Q; Dai H; Long Z; Tang B; Deng H; Chen Y; Zhang R; Zheng D; He Y; Xia K
J Hum Genet; 2002; 47(12):635-40. PubMed ID: 12522684
[TBL] [Abstract][Full Text] [Related]
12. Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss.
Gao X; Huang SS; Yuan YY; Wang GJ; Xu JC; Ji YB; Han MY; Yu F; Kang DY; Lin X; Dai P
Am J Med Genet A; 2015 Oct; 167A(10):2357-65. PubMed ID: 26079994
[TBL] [Abstract][Full Text] [Related]
13. Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1-2q23.3.
van Beelen E; Schraders M; Huygen PL; Oostrik J; Plantinga RF; van Drunen W; Collin RW; Kooper DP; Pennings RJ; Cremers CW; Kremer H; Kunst HP
Hear Res; 2013 Jun; 300():10-7. PubMed ID: 23538131
[TBL] [Abstract][Full Text] [Related]
14. Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.
Fagerheim T; Nilssen O; Raeymaekers P; Brox V; Moum T; Elverland HH; Teig E; Omland HH; Fostad GK; Tranebjaerg L
Hum Mol Genet; 1996 Aug; 5(8):1187-91. PubMed ID: 8842739
[TBL] [Abstract][Full Text] [Related]
15. Further evidence for a third deafness gene within the DFNA2 locus.
Goldstein JA; Lalwani AK
Am J Med Genet; 2002 Apr; 108(4):304-9. PubMed ID: 11920835
[TBL] [Abstract][Full Text] [Related]
16. DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.
Delmaghani S; Aghaie A; Compain-Nouaille S; Ataie A; Lemainque A; Zeinali S; Lathrop M; Weil D; Petit C
Eur J Hum Genet; 2003 Oct; 11(10):816-8. PubMed ID: 14512974
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.
Flex E; Mangino M; Mazzoli M; Martini A; Migliosi V; Colosimo A; Mingarelli R; Pizzuti A; Dallapiccola B
J Med Genet; 2003 Apr; 40(4):278-81. PubMed ID: 12676899
[TBL] [Abstract][Full Text] [Related]
19. Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
Verhoeven K; Fagerheim T; Prasad S; Wayne S; De Clau F; Balemans W; Verstreken M; Schatteman I; Solem B; Van de Heyning P; Tranebjärg L; Smith RJ; Van Camp G
Hum Genet; 2000 Jul; 107(1):7-11. PubMed ID: 10982027
[TBL] [Abstract][Full Text] [Related]
20. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.
Coucke P; Van Camp G; Djoyodiharjo B; Smith SD; Frants RR; Padberg GW; Darby JK; Huizing EH; Cremers CW; Kimberling WJ
N Engl J Med; 1994 Aug; 331(7):425-31. PubMed ID: 8035838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
