100 related articles for article (PubMed ID: 8766069)
1. [Genetic aspects of deafness].
Dallapiccola B; Mingarelli R; Gennarelli M; Novelli G
Acta Otorhinolaryngol Ital; 1996 Apr; 16(2):79-90. PubMed ID: 8766069
[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. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G
Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
[TBL] [Abstract][Full Text] [Related]
4. [Genetic study of sensorineural hearing loss].
Bliumina MG; Moskovkina AG
Genetika; 1982; 18(6):1012-7. PubMed ID: 7201942
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.
Cryns K; Pfister M; Pennings RJ; Bom SJ; Flothmann K; Caethoven G; Kremer H; Schatteman I; Köln KA; Tóth T; Kupka S; Blin N; Nürnberg P; Thiele H; van de Heyning PH; Reardon W; Stephens D; Cremers CW; Smith RJ; Van Camp G
Hum Genet; 2002 May; 110(5):389-94. PubMed ID: 12073007
[TBL] [Abstract][Full Text] [Related]
6. [Genetic characteristics of recessive sensorineural hearing loss].
Bliumina MG
Genetika; 1987 Oct; 23(10):1897-9. PubMed ID: 3692153
[TBL] [Abstract][Full Text] [Related]
7. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
8. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
9. [Mitochondrial DNA mutations and non-syndromic sensorineural hearing loss].
Kong W; Wang Q; Zheng X; Cheng H
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):338-42. PubMed ID: 12772452
[TBL] [Abstract][Full Text] [Related]
10. [Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].
Düzcan F; Wollnik B; Tepeli E; Ardiç FN; Uyguner O; Bağci H
Kulak Burun Bogaz Ihtis Derg; 2003 Sep; 11(3):85-8. PubMed ID: 14699249
[TBL] [Abstract][Full Text] [Related]
11. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
Chapiro E; Feldmann D; Denoyelle F; Sternberg D; Jardel C; Eliot MM; Bouccara D; Weil D; Garabédian EN; Couderc R; Petit C; Marlin S
Eur J Hum Genet; 2002 Dec; 10(12):851-6. PubMed ID: 12461693
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment.
López-Bigas N; Melchionda S; de Cid R; Grifa A; Zelante L; Govea N; Arbonés ML; Gasparini P; Estivill X
Hum Mutat; 2001 Dec; 18(6):548. PubMed ID: 11748854
[TBL] [Abstract][Full Text] [Related]
14. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).
McGuirt WT; Prasad SD; Griffith AJ; Kunst HP; Green GE; Shpargel KB; Runge C; Huybrechts C; Mueller RF; Lynch E; King MC; Brunner HG; Cremers CW; Takanosu M; Li SW; Arita M; Mayne R; Prockop DJ; Van Camp G; Smith RJ
Nat Genet; 1999 Dec; 23(4):413-9. PubMed ID: 10581026
[TBL] [Abstract][Full Text] [Related]
15. [From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].
Pennings RJ; Cryns K; Huygen PL; van Camp G; Cremers CW
Ned Tijdschr Geneeskd; 2003 Nov; 147(44):2170-2. PubMed ID: 14626834
[TBL] [Abstract][Full Text] [Related]
16. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
Alasti F; Sanati MH; Behrouzifard AH; Sadeghi A; de Brouwer AP; Kremer H; Smith RJ; Van Camp G
Int J Pediatr Otorhinolaryngol; 2008 Feb; 72(2):249-55. PubMed ID: 18022253
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
Usami S; Takahashi K; Yuge I; Ohtsuka A; Namba A; Abe S; Fransen E; Patthy L; Otting G; Van Camp G
Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.
Wagatsuma M; Kitoh R; Suzuki H; Fukuoka H; Takumi Y; Usami S
Clin Genet; 2007 Oct; 72(4):339-44. PubMed ID: 17850630
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]