129 related articles for article (PubMed ID: 8463117)
1. [Perspectives of molecular genetics of hearing disorders].
Kempf HG; Brändle TU
HNO; 1993 Feb; 41(2):68-76. PubMed ID: 8463117
[TBL] [Abstract][Full Text] [Related]
2. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
3. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area].
Oeken J; König E
HNO; 1993 Jun; 41(6):301-10. PubMed ID: 8365917
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genetic causes of hearing loss in children.
Cantani A
Padiatr Padol; 1989; 24(4):321-30. PubMed ID: 2694074
[TBL] [Abstract][Full Text] [Related]
6. Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation.
Lorda-Sanchez IJ; Ibañez AJ; Sanz RJ; Trujillo MJ; Anabitarte ME; Querejeta ME; Rodriguez de Alba M; Gimenez A; Infantes F; Ramos C; Garcia-Sandoval B; Ayuso C
Ophthalmic Genet; 2000 Sep; 21(3):185-9. PubMed ID: 11035551
[TBL] [Abstract][Full Text] [Related]
7. Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.
Schrijver I; Gardner P
Expert Rev Mol Diagn; 2006 May; 6(3):375-86. PubMed ID: 16706740
[TBL] [Abstract][Full Text] [Related]
8. Genetic approach to evaluation of hearing loss.
Cohen M; Phillips JA
Otolaryngol Clin North Am; 2012 Feb; 45(1):25-39. PubMed ID: 22115680
[TBL] [Abstract][Full Text] [Related]
9. Mouse models to study inner ear development and hereditary hearing loss.
Friedman LM; Dror AA; Avraham KB
Int J Dev Biol; 2007; 51(6-7):609-31. PubMed ID: 17891721
[TBL] [Abstract][Full Text] [Related]
10. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
Vieira H; Gregory-Evans K; Lim N; Brookes JL; Brueton LA; Gregory-Evans CY
Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
[TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
Kharrat M; Makni S; Makni K; Kammoun K; Charfeddine K; Azaeiz H; Jarraya F; Ben Hmida M; Gubler MC; Ayadi H; Hachicha J
Saudi J Kidney Dis Transpl; 2006 Sep; 17(3):320-5. PubMed ID: 16970251
[TBL] [Abstract][Full Text] [Related]
12. [Progress in genetic testing and prevention of hereditary hearing disorders].
Markova TG; Poliakov AV
Vestn Otorinolaringol; 2007; (4):7-10. PubMed ID: 17828104
[TBL] [Abstract][Full Text] [Related]
13. [Chromosome 15 satellite enlargement and hereditary deafness].
Zhuang J; Hu X; Zhang B
Zhonghua Er Bi Yan Hou Ke Za Zhi; 1994; 29(4):225-7. PubMed ID: 7803123
[TBL] [Abstract][Full Text] [Related]
14. Cracking the auditory genetic code: nonsyndromic hereditary hearing impairment.
Lalwani AK; Castelein CM
Am J Otol; 1999 Jan; 20(1):115-32. PubMed ID: 9918184
[TBL] [Abstract][Full Text] [Related]
15. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
Thirlwall AS; Brown DJ; McMillan PM; Barker SE; Lesperance MM
Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340
[TBL] [Abstract][Full Text] [Related]
16. A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
Govaerts PJ; De Ceulaer G; Daemers K; Verhoeven K; Van Camp G; Schatteman I; Verstreken M; Willems PJ; Somers T; Offeciers FE
Am J Otol; 1998 Nov; 19(6):718-23. PubMed ID: 9831143
[TBL] [Abstract][Full Text] [Related]
17. [Blepharophimosis, ptosis and epicanthus inversus syndrome plus sensorineural deafness].
Pérez-Caballero Macarrón C; Quintana Castilla A; Aparicio Meix JM
An Esp Pediatr; 1999 Nov; 51(5):530-2. PubMed ID: 10652806
[No Abstract] [Full Text] [Related]
18. [Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].
Espinós C; Pérez-Garrigues H; Beneyto M; Vilela C; Rodrigo O; Nájera C
An Otorrinolaringol Ibero Am; 1999; 26(1):83-95. PubMed ID: 10091368
[TBL] [Abstract][Full Text] [Related]
19. Vestibular and hearing loss in genetic and metabolic disorders.
Gasparini P; Estivill X; Fortina P
Curr Opin Neurol; 1999 Feb; 12(1):35-9. PubMed ID: 10097882
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
