226 related articles for article (PubMed ID: 17407011)
1. [Non-syndromic hereditary hearing impairment].
Birkenhäger R; Aschendorff A; Schipper J; Laszig R
Laryngorhinootologie; 2007 Apr; 86(4):299-309; quiz 310-3. PubMed ID: 17407011
[TBL] [Abstract][Full Text] [Related]
2. Deafness genes.
Kitamura K; Takahashi K; Tamagawa Y; Noguchi Y; Kuroishikawa Y; Ishikawa K; Hagiwara H
J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
[TBL] [Abstract][Full Text] [Related]
3. Hereditary deafness and phenotyping in humans.
Bitner-Glindzicz M
Br Med Bull; 2002; 63():73-94. PubMed ID: 12324385
[TBL] [Abstract][Full Text] [Related]
4. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
Schade G; Kothe C; Ruge G; Hess M; Meyer CG
Laryngorhinootologie; 2003 Jun; 82(6):397-401. PubMed ID: 12851846
[TBL] [Abstract][Full Text] [Related]
5. Non-syndromic, autosomal-recessive deafness.
Petersen MB; Willems PJ
Clin Genet; 2006 May; 69(5):371-92. PubMed ID: 16650073
[TBL] [Abstract][Full Text] [Related]
6. [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].
Birkenhäger R; Zimmer AJ; Maier W; Schipper J
Laryngorhinootologie; 2006 Mar; 85(3):191-6. PubMed ID: 16547895
[TBL] [Abstract][Full Text] [Related]
7. [Hereditary sensorineural deafness].
Denoyelle F; Marlin S; Petit C; Garabédian EN
Rev Prat; 2000 Jan; 50(2):146-9. PubMed ID: 10737085
[TBL] [Abstract][Full Text] [Related]
8. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.
Rabionet R; Gasparini P; Estivill X
Hum Mutat; 2000 Sep; 16(3):190-202. PubMed ID: 10980526
[TBL] [Abstract][Full Text] [Related]
9. Connexin mutation testing of children with nonsyndromic, autosomal recessive sensorineural hearing loss.
Thomas MA; Der Kaloustian VM; Tewfik TL
J Otolaryngol; 2004 Jun; 33(3):189-92. PubMed ID: 15841999
[TBL] [Abstract][Full Text] [Related]
10. Analysis of a cohort of children with sensory hearing loss using the SCALE systematic nomenclature.
Sculerati N
Laryngoscope; 2000 May; 110(5 Pt 1):787-98. PubMed ID: 10807358
[TBL] [Abstract][Full Text] [Related]
11. Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
Prasad S; Cucci RA; Green GE; Smith RJ
Hum Mutat; 2000 Dec; 16(6):502-8. PubMed ID: 11102979
[TBL] [Abstract][Full Text] [Related]
12. GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.
Najmabadi H; Cucci RA; Sahebjam S; Kouchakian N; Farhadi M; Kahrizi K; Arzhangi S; Daneshmandan N; Javan K; Smith RJ
Hum Mutat; 2002 May; 19(5):572. PubMed ID: 11968091
[TBL] [Abstract][Full Text] [Related]
13. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.
Kelsell DP; Dunlop J; Stevens HP; Lench NJ; Liang JN; Parry G; Mueller RF; Leigh IM
Nature; 1997 May; 387(6628):80-3. PubMed ID: 9139825
[TBL] [Abstract][Full Text] [Related]
14. The genetics of deafness.
Nance WE
Ment Retard Dev Disabil Res Rev; 2003; 9(2):109-19. PubMed ID: 12784229
[TBL] [Abstract][Full Text] [Related]
15. A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?
Pallares-Ruiz N; Blanchet P; Mondain M; Claustres M; Roux AF
Eur J Hum Genet; 2002 Jan; 10(1):72-6. PubMed ID: 11896458
[TBL] [Abstract][Full Text] [Related]
16. A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene.
Tamagawa Y; Kitamura K; Ishida T; Ishikawa K; Tanaka H; Tsuji S; Nishizawa M
Hum Mol Genet; 1996 Jun; 5(6):849-52. PubMed ID: 8776602
[TBL] [Abstract][Full Text] [Related]
17. Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.
Hutchin T; Coy NN; Conlon H; Telford E; Bromelow K; Blaydon D; Taylor G; Coghill E; Brown S; Trembath R; Liu XZ; Bitner-Glindzicz M; Mueller R
Clin Genet; 2005 Dec; 68(6):506-12. PubMed ID: 16283880
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.
Xia JH; Liu CY; Tang BS; Pan Q; Huang L; Dai HP; Zhang BR; Xie W; Hu DX; Zheng D; Shi XL; Wang DA; Xia K; Yu KP; Liao XD; Feng Y; Yang YF; Xiao JY; Xie DH; Huang JZ
Nat Genet; 1998 Dec; 20(4):370-3. PubMed ID: 9843210
[TBL] [Abstract][Full Text] [Related]
19. Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.
Mesolella M; Tranchino G; Nardone M; Motta S; Galli V
Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):995-1005. PubMed ID: 15236885
[TBL] [Abstract][Full Text] [Related]
20. [Study of a mutation in connexin 26 gene associated with congenital sensorineural deafness].
Wang P; Wang Y; Liu X; Du B
Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2001 Oct; 15(10):439-41. PubMed ID: 12541685
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]