Showing results (121-130 of 158) with videos related to
Sort By:
Pageof 16
Archives of Otolaryngology (Chicago, Ill. : 1960)|May 1, 1983
Interferons and bronchogenic carcinoma in juvenile laryngeal papillomatosisT J Schouten, P van den Broek, C W Cremers, et al.International Journal of Pediatric Otorhinolaryngology|June 9, 2001
The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family studyC Stinckens, L Standaert, J W Casselman, et al.The Annals of Otology, Rhinology, and Laryngology|December 1, 1996
Stable and progressive hearing loss in type 2A Usher's syndromeA van Aarem, A J Pinckers, W J Kimberling, et al.Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.Human Mutation|September 30, 1999
Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.Clinical Otolaryngology and Allied Sciences|February 15, 2002
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a familyW I Verhagen, S J Bom, E Fransen, et al.Human Mutation|May 29, 1998
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndromeS Kumar, W J Kimberling, M D Weston, et al.Ophthalmic Genetics|December 1, 1995
Ophthalmologic findings in Usher syndrome type 2AA Van Aarem, M Wagenaar, A J Pinckers, et al.Genomics|January 1, 1996
Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8qS Kumar, W J Kimberling, A Lanyi, et al.Journal of Medical Genetics|April 4, 2000
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5qS Pieke-Dahl, C G Möller, P M Kelley, et al.Pageof 16