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R J Smith

Showing results (611-620 of 636) with videos related to

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Radiology|August 1, 1982
NMR imaging of forearms in healthy volunteers and patients with giant-cell tumor of boneT J Brady, M C Gebhardt, I L Pykett, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.
Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.
Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.
Scientific Reports|February 9, 2021
Evaluating very high energy electron RBE from nanodosimetric pBR322 plasmid DNA damageK L Small, N T Henthorn, D Angal-Kalinin, et al.
Pageof 64

Showing results (611-620 of 636) with videos related to

Sort By:
Pageof 64
Radiology|August 1, 1982
NMR imaging of forearms in healthy volunteers and patients with giant-cell tumor of boneT J Brady, M C Gebhardt, I L Pykett, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.
Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.
Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.
Scientific Reports|February 9, 2021
Evaluating very high energy electron RBE from nanodosimetric pBR322 plasmid DNA damageK L Small, N T Henthorn, D Angal-Kalinin, et al.
Pageof 64