HuGE Literature Finder
Records 1-6
|
Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2018 Jul 39 (6): 732-738. Boudewyns An, van den Ende Jenneke, Sommen Manou, Wuyts Wim, Peeters Nils, Van de Heyning Paul, Van Camp G |
|
Does congenital cytomegalovirus infection lead to hearing loss by inducing mutation of the GJB2 gene?
Pediatric research 2013 Aug 74 (2): 121-6. Li Lu-Quan, Tan Jun-Jie, Zhou Yuan, Yu Jia-L |
|
Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patients.
Advances in medical sciences 2013 58 (2): 419-28. Teek R, Kruustük K, Žordania R, Joost K, Kahre T, Tõnisson N, Nelis M, Zilina O, Tranebjaerg L, Reimand T, Ounap |
|
Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalities.
Archives of otolaryngology--head & neck surgery 2010 Oct 136 (10): 999-1004. Kimani Jane W, Buchman Craig A, Booker Jessica K, Huang Benjamin Y, Castillo Mauricio, Powell Cynthia M, Weck Karen |
|
Genetic analysis of presbycusis by arrayed primer extension.
Annals of clinical and laboratory science 2008 38 (4): 352-60. Rodriguez-Paris Juan, Ballay Charles, Inserra Michelle, Stidham Katrina, Colen Tahl, Roberson Joseph, Gardner Phyllis, Schrijver Ir |
|
GJB2 and GJB6 mutations in children with congenital cytomegalovirus infection.
Pediatric research 2007 Jun 61 (6): 687-91. Ross Shannon A, Novak Zdenek, Kumbla Rekha A, Zhang Kui, Fowler Karen B, Boppana Sure |
- Page last reviewed:Oct 1, 2020
- Page last updated:Jan 15, 2021
- Content source: