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Journal Abstract Search
247 related items for PubMed ID: 6990581
1. [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children]. Bliumina MG, Moskovkina AG. Vestn Otorinolaringol; 1980; (1):67-73. PubMed ID: 6990581 [No Abstract] [Full Text] [Related]
4. [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 [Abstract] [Full Text] [Related]
5. Hereditary hearing loss. Arnos KS. N Engl J Med; 1994 Aug 18; 331(7):469-70. PubMed ID: 8035845 [No Abstract] [Full Text] [Related]
6. Heredity hearing losses with delayed onset: mechanisms of expression. Jahn AF, Noyek AM. Otolaryngol Clin North Am; 1981 Feb 18; 14(1):59-64. PubMed ID: 6789283 [Abstract] [Full Text] [Related]
7. [Hereditary hearing loss: new diagnostic possibilities]. Hergersberg M, Weigell-Weber M. Schweiz Med Wochenschr; 2000 Apr 01; 130(13):485-9. PubMed ID: 10812644 [Abstract] [Full Text] [Related]
8. [Genetic deafness:the primary cause of sensorineural hearing loss in children]. Lina-Granade G, Morlé L, Alloisio N, Edery P, Plauchu H, Truy E, Disant F, Collet L. Arch Pediatr; 2001 Mar 01; 8(3):308-12. PubMed ID: 11270257 [Abstract] [Full Text] [Related]
9. [Etiologic problems of hearing disorders in "risk children"]. Beckmann G. HNO; 1969 Aug 01; 17(8):225-9. PubMed ID: 4996331 [No Abstract] [Full Text] [Related]
10. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation. Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S. Auris Nasus Larynx; 2005 Jun 01; 32(2):119-24. PubMed ID: 15917167 [Abstract] [Full Text] [Related]
11. Genetic hearing loss. Keogh IJ, Godinho RN. Ir Med J; 2002 Jan 01; 95(1):5-7. PubMed ID: 11928792 [No Abstract] [Full Text] [Related]
12. [Molecular analysis of the heterogeneity of hereditary monosymptomatic sensorineural hearing loss]. Fiegert P, Lamprecht-Dinnesen A, Preisler-Adams S, Deufel T. Laryngorhinootologie; 1996 Mar 01; 75(3):141-7. PubMed ID: 8652029 [Abstract] [Full Text] [Related]
13. 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 01; 10(3):210-2. PubMed ID: 11973626 [Abstract] [Full Text] [Related]
14. A pedigree with Pendred syndrome: case report and discussion on hereditary hearing loss. Hiyoshi M, Yamane H. Acta Otolaryngol Suppl; 2004 Oct 01; (554):45-6. PubMed ID: 15513511 [Abstract] [Full Text] [Related]
15. [Importance of audiological examinations of hearing parents of children with congenital hearing defects of undetermined origin]. Courtoy M, Hennebert D, Perier O, Van den Haute J. Acta Otorhinolaryngol Belg; 1972 Oct 01; 26(6):629-34. PubMed ID: 4669676 [No Abstract] [Full Text] [Related]
16. Symposium on sensorineural hearing loss in children: early detection and intervention. Evaluation of the child with sensorineural hearing impairment. Linthicum FH. Otolaryngol Clin North Am; 1975 Feb 01; 8(1):69-75. PubMed ID: 1167956 [Abstract] [Full Text] [Related]
17. Inheritance of hearing defects in pupils of school for children with hearing handicap in Horicky. Hybásek I, Prsiková I. Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1980 Feb 01; 23(2):185-96. PubMed ID: 6970402 [No Abstract] [Full Text] [Related]
18. [Etiology of neurosensory hearing loss in children with normal-hearing parents]. Bliumina MG, Moskovkina AG. Vestn Otorinolaringol; 1982 Feb 01; (1):23-6. PubMed ID: 7064276 [No Abstract] [Full Text] [Related]
19. Genetic causes of nonsyndromic hearing loss. Skvorak Giersch AB, Morton CC. Curr Opin Pediatr; 1999 Dec 01; 11(6):551-7. PubMed ID: 10590915 [Abstract] [Full Text] [Related]
20. Hearing impairment susceptibility in elderly men and the DFNA18 locus. Garringer HJ, Pankratz ND, Nichols WC, Reed T. Arch Otolaryngol Head Neck Surg; 2006 May 01; 132(5):506-10. PubMed ID: 16702566 [Abstract] [Full Text] [Related] Page: [Next] [New Search]