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Aetiological investigations of hearing loss in childhood: a review.
Bamiou DE, MacArdle B, Bitner-Glindzicz M, Sirimanna T. Bamiou DE, et al. Clin Otolaryngol Allied Sci. 2000 Apr;25(2):98-106. doi: 10.1046/j.1365-2273.2000.00346.x. Clin Otolaryngol Allied Sci. 2000. PMID: 10816211 Review. No abstract available.
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, Hussain K, Furth-Lavi J, Cosgrove KE, Shepherd RM, Barnes PD, O'Brien RE, Farndon PA, Sowden J, Liu XZ, Scanlan MJ, Malcolm S, Dunne MJ, Aynsley-Green A, Glaser B. Bitner-Glindzicz M, et al. Nat Genet. 2000 Sep;26(1):56-60. doi: 10.1038/79178. Nat Genet. 2000. PMID: 10973248
Late postnatal onset of hearing loss due to GJB2 mutations.
Pagarkar W, Bitner-Glindzicz M, Knight J, Sirimanna T. Pagarkar W, et al. Int J Pediatr Otorhinolaryngol. 2006 Jun;70(6):1119-24. doi: 10.1016/j.ijporl.2005.10.026. Epub 2006 Feb 15. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16469394
139 results