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William J Kimberling

Showing results (1-10 of 56) with videos related to

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Audiology & Neuro-Otology|December 17, 2003
Transcription, translation, and transitionsWilliam J Kimberling
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Uncertainties in the molecular diagnosis of recessive hearing loss disordersWilliam J Kimberling
Human Mutation|September 8, 2005
Estimation of the frequency of occult mutations for an autosomal recessive disease in the presence of genetic heterogeneity: application to genetic hearing loss disordersWilliam J Kimberling
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hearing loss disorders associated with renal diseaseWilliam J Kimberling, Nicolo Borsa, Richard J H Smith
Molecular Vision|December 14, 2004
Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7AArun Kumar, Mohan Babu, William J Kimberling, et al.
The Annals of Otology, Rhinology, and Laryngology|December 25, 2002
Hearing loss in Usher syndrome type II is nonprogressiveChristoph F V Reisser, William J Kimberling, Christian R Otterstedde
Ophthalmic Genetics|December 23, 2010
Phenotypes in defined genotypes including siblings with Usher syndromeEva Malm, Vesna Ponjavic, Claes Möller, et al.
Acta Ophthalmologica Scandinavica|August 2, 2006
Longterm visual prognosis in Usher syndrome types 1 and 2André M Sadeghi, Kristina Eriksson, William J Kimberling, et al.
Hearing Research|January 15, 2002
Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIaGautam Bhattacharya, Caroline Miller, William J Kimberling, et al.
Journal of Cell Science|December 17, 2003
A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructureGautam Bhattacharya, Raghu Kalluri, Dana J Orten, et al.
Pageof 6

Showing results (1-10 of 56) with videos related to

Sort By:
Pageof 6
Audiology & Neuro-Otology|December 17, 2003
Transcription, translation, and transitionsWilliam J Kimberling
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Uncertainties in the molecular diagnosis of recessive hearing loss disordersWilliam J Kimberling
Human Mutation|September 8, 2005
Estimation of the frequency of occult mutations for an autosomal recessive disease in the presence of genetic heterogeneity: application to genetic hearing loss disordersWilliam J Kimberling
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hearing loss disorders associated with renal diseaseWilliam J Kimberling, Nicolo Borsa, Richard J H Smith
Molecular Vision|December 14, 2004
Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7AArun Kumar, Mohan Babu, William J Kimberling, et al.
The Annals of Otology, Rhinology, and Laryngology|December 25, 2002
Hearing loss in Usher syndrome type II is nonprogressiveChristoph F V Reisser, William J Kimberling, Christian R Otterstedde
Ophthalmic Genetics|December 23, 2010
Phenotypes in defined genotypes including siblings with Usher syndromeEva Malm, Vesna Ponjavic, Claes Möller, et al.
Acta Ophthalmologica Scandinavica|August 2, 2006
Longterm visual prognosis in Usher syndrome types 1 and 2André M Sadeghi, Kristina Eriksson, William J Kimberling, et al.
Hearing Research|January 15, 2002
Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIaGautam Bhattacharya, Caroline Miller, William J Kimberling, et al.
Journal of Cell Science|December 17, 2003
A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructureGautam Bhattacharya, Raghu Kalluri, Dana J Orten, et al.
Pageof 6