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240 related items for PubMed ID: 9765703
1. [Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people]. Marlin S, Denoyelle F, Garabédian EN, Petit C. Ann Otolaryngol Chir Cervicofac; 1998 Feb; 115(1):3-8. PubMed ID: 9765703 [Abstract] [Full Text] [Related]
2. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population. Riga M, Psarommatis I, Lyra Ch, Douniadakis D, Tsakanikos M, Neou P, Apostolopoulos N. Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280 [Abstract] [Full Text] [Related]
4. Genetic counseling for the deaf. Arnos KS, Israel J, Devlin L, Wilson MP. Otolaryngol Clin North Am; 1992 Oct; 25(5):953-71. PubMed ID: 1408198 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. [Etiological, clinical and neuroradiological investigation of deaf children with additional neuropsychiatric disabilities]. Chilosi AM, Scusa MF, Comparini A, Genovese E, Forli F, Berrettini S, Cipriani P. Minerva Pediatr; 2012 Apr; 64(2):213-23. PubMed ID: 22495195 [Abstract] [Full Text] [Related]
7. Parental attitudes toward genetic testing for prelingual deafness in China. Fu S, Dong J, Wang C, Chen G. Int J Pediatr Otorhinolaryngol; 2010 Oct; 74(10):1122-5. PubMed ID: 20637511 [Abstract] [Full Text] [Related]
8. [Hearing impairment and psychopathological disorders in children and adolescents. Review of the recent literature]. Bailly D, Dechoulydelenclave MB, Lauwerier L. Encephale; 2003 Oct; 29(4 Pt 1):329-37. PubMed ID: 14615703 [Abstract] [Full Text] [Related]
9. Evaluation of deaf children in a large series in Turkey. Ozturk O, Silan F, Oghan F, Egeli E, Belli S, Tokmak A, Egeli A, Harputluoglu U, Onder HI, Zafer C. Int J Pediatr Otorhinolaryngol; 2005 Mar; 69(3):367-73. PubMed ID: 15733596 [Abstract] [Full Text] [Related]
10. Genetic selection for deafness: the views of hearing children of deaf adults. Mand C, Duncan RE, Gillam L, Collins V, Delatycki MB. J Med Ethics; 2009 Dec; 35(12):722-8. PubMed ID: 19948926 [Abstract] [Full Text] [Related]
11. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness. Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX. Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862 [Abstract] [Full Text] [Related]
12. On the etiology of hearing loss in a population of 155 institutionalized children. Dereymaeker AM, Fryns JP, Ars B, Andrescescou J, Van den Berghe H. Acta Otorhinolaryngol Belg; 1991 Feb 03; 45(3):283-91. PubMed ID: 1659109 [Abstract] [Full Text] [Related]
13. Syndromic etiology in children at schools for the deaf in Turkey. Silan F, Demirci L, Egeli A, Egeli E, Onder HI, Ozturk O, Unal ZS. Int J Pediatr Otorhinolaryngol; 2004 Nov 03; 68(11):1399-406. PubMed ID: 15488971 [Abstract] [Full Text] [Related]
14. [Analysis of 104 children with hearing defects (author's transl)]. Plöchl E, Tasser C. Padiatr Padol; 1980 Nov 03; 15(4):375-84. PubMed ID: 7193320 [Abstract] [Full Text] [Related]
15. Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists. Parker MJ, Fortnum H, Young ID, Davis AC. J Med Genet; 1999 Feb 03; 36(2):125-30. PubMed ID: 10051011 [Abstract] [Full Text] [Related]
16. Aetiology of childhood hearing loss in Cameroon (sub-Saharan Africa). Wonkam A, Noubiap JJ, Djomou F, Fieggen K, Njock R, Toure GB. Eur J Med Genet; 2013 Jan 03; 56(1):20-5. PubMed ID: 23085303 [Abstract] [Full Text] [Related]
17. 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 03; 10(12):851-6. PubMed ID: 12461693 [Abstract] [Full Text] [Related]
18. [Congenital and hereditary hearing disorders in population of the Nakhichevan Autonomous Republic]. Panakhiian VM. Vestn Otorinolaringol; 2004 Dec 03; (6):22-4. PubMed ID: 15699983 [Abstract] [Full Text] [Related]
19. [Hereditary progressive sensorineural deafness--report of 30 cases in 12 families]. Wang X. Zhonghua Yi Xue Za Zhi; 1983 Nov 03; 63(11):694-8. PubMed ID: 6426737 [No Abstract] [Full Text] [Related]
20. Alport syndrome. Molecular genetic aspects. Hertz JM. Dan Med Bull; 2009 Aug 03; 56(3):105-52. PubMed ID: 19728970 [Abstract] [Full Text] [Related] Page: [Next] [New Search]