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2. [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. Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss. Nance WE; Lim BG; Dodson KM J Clin Virol; 2006 Feb; 35(2):221-5. PubMed ID: 16384744 [TBL] [Abstract][Full Text] [Related]
5. A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I. Otterstedde CR; Spandau U; Blankenagel A; Kimberling WJ; Reisser C Laryngoscope; 2001 Jan; 111(1):84-6. PubMed ID: 11192904 [TBL] [Abstract][Full Text] [Related]
6. [Hearing loss among handicapped persons]. Bouccara D; Sterkers O Rev Prat; 2009 May; 59(5):653-6. PubMed ID: 19552204 [TBL] [Abstract][Full Text] [Related]
7. Evaluation of ESPN, MYO3A, SLC26A5 and USH1C as candidates for hereditary non-syndromic deafness (congenital sensorineural deafness) in Dalmatian dogs. Mieskes K; Distl O Anim Genet; 2007 Oct; 38(5):533-4. PubMed ID: 17614983 [No Abstract] [Full Text] [Related]
8. Sensorineural hearing loss in children. Classification and evaluation. Chan KH Otolaryngol Clin North Am; 1994 Jun; 27(3):473-86. PubMed ID: 8065754 [TBL] [Abstract][Full Text] [Related]
10. [Congenital and hereditary hearing disorders in population of the Nakhichevan Autonomous Republic]. Panakhiian VM Vestn Otorinolaringol; 2004; (6):22-4. PubMed ID: 15699983 [TBL] [Abstract][Full Text] [Related]
11. Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalities. Tekin M; Fitoz S; Arici S; Cetinkaya E; Incesulu A Int J Pediatr Otorhinolaryngol; 2006 May; 70(5):885-9. PubMed ID: 16325926 [TBL] [Abstract][Full Text] [Related]
12. [Genetic study of sensorineural hearing loss]. Bliumina MG; Moskovkina AG Genetika; 1982; 18(6):1012-7. PubMed ID: 7201942 [TBL] [Abstract][Full Text] [Related]
13. Sensorineural hearing loss in insulin-like growth factor I-null mice: a new model of human deafness. Cediel R; Riquelme R; Contreras J; Díaz A; Varela-Nieto I Eur J Neurosci; 2006 Jan; 23(2):587-90. PubMed ID: 16420467 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Syndromal approaches to the nosology of hereditary deafness. Konigsmark BW Birth Defects Orig Artic Ser; 1971 Mar; 07(4):2-17. PubMed ID: 5173348 [TBL] [Abstract][Full Text] [Related]
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19. [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]
20. Deafness linked to DFNA2: one locus but how many genes? Van Hauwe P; Coucke PJ; Declau F; Kunst H; Ensink RJ; Marres HA; Cremers CW; Djelantik B; Smith SD; Kelley P; Van de Heyning PH; Van Camp G Nat Genet; 1999 Mar; 21(3):263. PubMed ID: 10080176 [No Abstract] [Full Text] [Related] [Next] [New Search]