Genetic testing to identify deaf newborns
- PMID: 10979110
- DOI: 10.1001/jama.284.10.1245
Genetic testing to identify deaf newborns
Similar articles
-
Mutation screening for deafness: more than simply another diagnostic test.Arch Otolaryngol Head Neck Surg. 2001 Aug;127(8):941-2. doi: 10.1001/archotol.127.8.941. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11493202 No abstract available.
-
Deafness and mutations in the connexin 26 gene.N Engl J Med. 1999 Apr 22;340(16):1288. doi: 10.1056/nejm199904223401614. N Engl J Med. 1999. PMID: 10215495 No abstract available.
-
[Genetic diagnosis of deafness].Nihon Rinsho. 2005 Dec;63 Suppl 12:258-63. Nihon Rinsho. 2005. PMID: 16416804 Review. Japanese. No abstract available.
-
Genetic evaluation and counseling for congenital deafness.Adv Otorhinolaryngol. 2002;61:230-40. doi: 10.1159/000066814. Adv Otorhinolaryngol. 2002. PMID: 12408089 No abstract available.
-
Genetic screening for deafness.Pediatr Clin North Am. 2003 Apr;50(2):315-29. doi: 10.1016/s0031-3955(03)00026-9. Pediatr Clin North Am. 2003. PMID: 12809325 Review.
Cited by
-
Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.J Mol Diagn. 2004 Nov;6(4):275-84. doi: 10.1016/S1525-1578(10)60522-3. J Mol Diagn. 2004. PMID: 15507665 Free PMC article. Review.
-
DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes.Front Mol Neurosci. 2017 Dec 22;10:428. doi: 10.3389/fnmol.2017.00428. eCollection 2017. Front Mol Neurosci. 2017. PMID: 29311818 Free PMC article. Review.
-
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.J Pers Med. 2022 Nov 4;12(11):1843. doi: 10.3390/jpm12111843. J Pers Med. 2022. PMID: 36579563 Free PMC article.
-
Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.Arch Otolaryngol Head Neck Surg. 2010 Jan;136(1):81-7. doi: 10.1001/archoto.2009.202. Arch Otolaryngol Head Neck Surg. 2010. PMID: 20083784 Free PMC article.
-
Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population.PLoS One. 2015 Jun 10;10(6):e0125416. doi: 10.1371/journal.pone.0125416. eCollection 2015. PLoS One. 2015. PMID: 26061264 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical