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Audiology & Neuro-Otology
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December 17, 2003
Transcription, translation, and transitions
William 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 disorders
William 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 disorders
William J Kimberling
Advances in Oto-Rhino-Laryngology
|
March 2, 2011
Hearing loss disorders associated with renal disease
William 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 MYO7A
Arun 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 nonprogressive
Christoph F V Reisser, William J Kimberling, Christian R Otterstedde
Ophthalmic Genetics
|
December 23, 2010
Phenotypes in defined genotypes including siblings with Usher syndrome
Eva Malm, Vesna Ponjavic, Claes Möller, et al.
Acta Ophthalmologica Scandinavica
|
August 2, 2006
Longterm visual prognosis in Usher syndrome types 1 and 2
André 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 IIa
Gautam 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 superstructure
Gautam Bhattacharya, Raghu Kalluri, Dana J Orten, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 56) with videos related to
Sort By:
Page
of 6
Audiology & Neuro-Otology
|
December 17, 2003
Transcription, translation, and transitions
William 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 disorders
William 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 disorders
William J Kimberling
Advances in Oto-Rhino-Laryngology
|
March 2, 2011
Hearing loss disorders associated with renal disease
William 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 MYO7A
Arun 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 nonprogressive
Christoph F V Reisser, William J Kimberling, Christian R Otterstedde
Ophthalmic Genetics
|
December 23, 2010
Phenotypes in defined genotypes including siblings with Usher syndrome
Eva Malm, Vesna Ponjavic, Claes Möller, et al.
Acta Ophthalmologica Scandinavica
|
August 2, 2006
Longterm visual prognosis in Usher syndrome types 1 and 2
André 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 IIa
Gautam 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 superstructure
Gautam Bhattacharya, Raghu Kalluri, Dana J Orten, et al.
Page
of 6