169 related articles for article (PubMed ID: 10424813)
1. A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.
Van Camp G; Kunst H; Flothmann K; McGuirt W; Wauters J; Marres H; Verstreken M; Bespalova IN; Burmeister M; Van de Heyning PH; Smith RJ; Willems PJ; Cremers CW; Lesperance MM
J Med Genet; 1999 Jul; 36(7):532-6. PubMed ID: 10424813
[TBL] [Abstract][Full Text] [Related]
2. A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
Bönsch D; Scheer P; Neumann C; Lang-Roth R; Seifert E; Storch P; Weiller C; Lamprecht-Dinnesen A; Deufel T
Eur J Hum Genet; 2001 Mar; 9(3):165-70. PubMed ID: 11313754
[TBL] [Abstract][Full Text] [Related]
3. Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family.
Komatsu K; Nakamura N; Ghadami M; Matsumoto N; Kishino T; Ohta T; Niikawa N; Yoshiura K
J Hum Genet; 2002; 47(8):395-9. PubMed ID: 12181639
[TBL] [Abstract][Full Text] [Related]
4. Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment.
Tóth T; Pfister M; Zenner HP; Sziklai I
Int J Pediatr Otorhinolaryngol; 2006 Feb; 70(2):201-6. PubMed ID: 16043233
[TBL] [Abstract][Full Text] [Related]
5. Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3.
Brodwolf S; Böddeker IR; Ziegler A; Rausch P; Kunz J
Clin Genet; 2001 Aug; 60(2):155-60. PubMed ID: 11553051
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.
Farah WI; Aminuddin BS; Ruszymah BH
Malays J Pathol; 2006 Jun; 28(1):23-33. PubMed ID: 17694956
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
Modamio-Høybjør S; Moreno-Pelayo MA; Mencía A; del Castillo I; Chardenoux S; Armenta D; Lathrop M; Petit C; Moreno F
Hum Genet; 2003 Jan; 112(1):24-8. PubMed ID: 12483295
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.
Morell RJ; Friderici KH; Wei S; Elfenbein JL; Friedman TB; Fisher RA
Genomics; 2000 Jan; 63(1):1-6. PubMed ID: 10662538
[TBL] [Abstract][Full Text] [Related]
13. A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD.
Pfister MH; Apaydin F; Turan O; Bereketoglu M; Bylgen V; Braendle U; Zenner HP; Lalwani AK
Genomics; 1998 Nov; 53(3):377-82. PubMed ID: 9799605
[TBL] [Abstract][Full Text] [Related]
14. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
Tlili A; Masmoudi S; Dhouib H; Bouaziz S; Rebeh IB; Chouchen J; Turki K; Benzina Z; Charfedine I; Drira M; Ayadi H
Ann Hum Genet; 2007 Mar; 71(Pt 2):271-5. PubMed ID: 17166180
[TBL] [Abstract][Full Text] [Related]
15. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
Mustapha M; Chouery E; Chardenoux S; Naboulsi M; Paronnaud J; Lemainque A; Mégarbané A; Loiselet J; Weil D; Lathrop M; Petit C
Eur J Hum Genet; 2002 Mar; 10(3):210-2. PubMed ID: 11973626
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
Nürnberg G; Jacobi FK; Broghammer M; Becker C; Blin N; Nürnberg P; Stephani U; Pusch CM
Int J Mol Med; 2008 Apr; 21(4):429-38. PubMed ID: 18360688
[TBL] [Abstract][Full Text] [Related]
18. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
Manolis EN; Eavey RD; Sangwatanaroj S; Halpin C; Rosenbaum S; Watkins H; Jarcho J; Seidman CE; Seidman JG
Am J Otol; 1999 Sep; 20(5):621-6. PubMed ID: 10503584
[TBL] [Abstract][Full Text] [Related]
19. Physical mapping of the mouse tilted locus identifies an association between human deafness loci DFNA6/14 and vestibular system development.
Hurle B; Lane K; Kenney J; Tarantino LM; Bucan M; Brownstein BH; Ornitz DM
Genomics; 2001 Oct; 77(3):189-99. PubMed ID: 11597144
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study.
Bom SJ; Van Camp G; Cryns K; Admiraal RJ; Huygen PL; Cremers CW
Otol Neurotol; 2002 Nov; 23(6):876-84. PubMed ID: 12438850
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
