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R J Smith

Showing results (571-580 of 636) with videos related to

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Archives of Otolaryngology--Head & Neck Surgery|January 24, 1998
Presymptomatic diagnosis of nonsyndromic hearing loss by genotypingA H Chen, R F Mueller, S D Prasad, et al.
Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
Annals of Internal Medicine|May 15, 1992
Clinical and metabolic efficacy of glutamine-supplemented parenteral nutrition after bone marrow transplantation. A randomized, double-blind, controlled studyT R Ziegler, L S Young, K Benfell, et al.
Microbial Drug Resistance (Larchmont, N.Y.)|October 1, 1995
Risk factor assessment for the acquisition of fluoroquinolone-resistant isolates of Pseudomonas aeruginosa in a community-based hospitalL M Baddour, D V Hicks, M M Tayidi, et al.
American Journal of Medical Genetics|March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome ConsortiumR J Smith, C I Berlin, J F Hejtmancik, et al.
Human Molecular Genetics|October 1, 1995
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3M M Lesperance, J W Hall, F H Bess, et al.
Human Molecular Genetics|February 13, 2001
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15A H Chen, D A Stephan, T Hasson, et al.
The American Journal of Physiology|December 1, 1995
Resection-induced colonic adaptation is augmented by IGF-I and associated with upregulation of colonic IGF-I mRNAM P Mantell, T R Ziegler, W T Adamson, et al.
Pageof 64

Showing results (571-580 of 636) with videos related to

Sort By:
Pageof 64
Archives of Otolaryngology--Head & Neck Surgery|January 24, 1998
Presymptomatic diagnosis of nonsyndromic hearing loss by genotypingA H Chen, R F Mueller, S D Prasad, et al.
Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
Annals of Internal Medicine|May 15, 1992
Clinical and metabolic efficacy of glutamine-supplemented parenteral nutrition after bone marrow transplantation. A randomized, double-blind, controlled studyT R Ziegler, L S Young, K Benfell, et al.
Microbial Drug Resistance (Larchmont, N.Y.)|October 1, 1995
Risk factor assessment for the acquisition of fluoroquinolone-resistant isolates of Pseudomonas aeruginosa in a community-based hospitalL M Baddour, D V Hicks, M M Tayidi, et al.
American Journal of Medical Genetics|March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome ConsortiumR J Smith, C I Berlin, J F Hejtmancik, et al.
Human Molecular Genetics|October 1, 1995
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3M M Lesperance, J W Hall, F H Bess, et al.
Human Molecular Genetics|February 13, 2001
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15A H Chen, D A Stephan, T Hasson, et al.
The American Journal of Physiology|December 1, 1995
Resection-induced colonic adaptation is augmented by IGF-I and associated with upregulation of colonic IGF-I mRNAM P Mantell, T R Ziegler, W T Adamson, et al.
Pageof 64