These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Diagnosis, Intervention, and Prevention of Genetic Hearing Loss. Yang T; Guo L; Wang L; Yu X Adv Exp Med Biol; 2019; 1130():73-92. PubMed ID: 30915702 [TBL] [Abstract][Full Text] [Related]
6. Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness. Xia W; Liu F; Ma D Front Med; 2016 Jun; 10(2):137-42. PubMed ID: 27142990 [TBL] [Abstract][Full Text] [Related]
7. Congenital and acquired cytomegalovirus infection and hearing evaluation in children. Smiechura M; Strużycka M; Konopka W Otolaryngol Pol; 2014; 68(6):303-7. PubMed ID: 25308607 [TBL] [Abstract][Full Text] [Related]
8. Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness. Martinez A; Linden J; Schimmenti LA; Palmer CG Genet Med; 2003; 5(2):106-12. PubMed ID: 12644780 [TBL] [Abstract][Full Text] [Related]
9. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Liu XZ; Walsh J; Mburu P; Kendrick-Jones J; Cope MJ; Steel KP; Brown SD Nat Genet; 1997 Jun; 16(2):188-90. PubMed ID: 9171832 [TBL] [Abstract][Full Text] [Related]
10. [Clinical practice guidelines for hereditary non-syndromic deafness]. Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association ; Yuan H; Dai P; Liu Y; Yang T Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):269-276. PubMed ID: 32128743 [TBL] [Abstract][Full Text] [Related]
14. 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 [TBL] [Abstract][Full Text] [Related]
15. Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations. Shaukat S; Fatima Z; Zehra U; Waqar AB J Ayub Med Coll Abbottabad; 2003; 15(3):59-64. PubMed ID: 14727345 [TBL] [Abstract][Full Text] [Related]
16. Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation. Mesolella M; Tranchino G; Nardone M; Motta S; Galli V Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):995-1005. PubMed ID: 15236885 [TBL] [Abstract][Full Text] [Related]
17. [Early diagnosis of congenital hearing loss. Use of oto-acoustic emission tests in newborn infants with increased risk of hearing impairment]. Størdal K; Anderssen SH; Lunde JT; Andersen R; Sponheim L Tidsskr Nor Laegeforen; 1998 Oct; 118(26):4076-8. PubMed ID: 9844511 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment. Qu R; Sang Q; Xu Y; Feng R; Jin L; He L; Wang L Int J Pediatr Otorhinolaryngol; 2016 May; 84():43-7. PubMed ID: 27063751 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. [Genetics of hearing disorders in children]. Paoloni-Giacobino A; Ranza E; Abramowicz M; Senn P; Cao Van H Rev Med Suisse; 2019 Oct; 15(665):1740-1745. PubMed ID: 31580017 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]