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G van Camp

Showing results (161-170 of 214) with videos related to

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Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Genes and Immunity|February 26, 2010
Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2I Schrauwen, K Venken, K Vanderstraeten, et al.
Clinical Genetics|April 8, 2011
A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44I Schrauwen, N J D Weegerink, E Fransen, et al.
Endocrine-Related Cancer|July 20, 2018
Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasmsT Vandamme, M Beyens, G Boons, et al.
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Neuropharmacology|March 27, 2018
The reduction in glutamate release is predictive of cognitive and emotional alterations that are corrected by the positive modulator of AMPA receptors S 47445 in perinatal stressed ratsS Morley-Fletcher, A R Zuena, J Mairesse, et al.
Annals of Human Genetics|February 12, 2009
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patientsM Thys, I Schrauwen, K Vanderstraeten, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
International Journal of Pediatric Otorhinolaryngology|December 22, 1999
Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findingsR F Mueller, A Nehammer, A Middleton, et al.
Genomics|February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, et al.
Pageof 22

Showing results (161-170 of 214) with videos related to

Sort By:
Pageof 22
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Genes and Immunity|February 26, 2010
Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2I Schrauwen, K Venken, K Vanderstraeten, et al.
Clinical Genetics|April 8, 2011
A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44I Schrauwen, N J D Weegerink, E Fransen, et al.
Endocrine-Related Cancer|July 20, 2018
Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasmsT Vandamme, M Beyens, G Boons, et al.
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Neuropharmacology|March 27, 2018
The reduction in glutamate release is predictive of cognitive and emotional alterations that are corrected by the positive modulator of AMPA receptors S 47445 in perinatal stressed ratsS Morley-Fletcher, A R Zuena, J Mairesse, et al.
Annals of Human Genetics|February 12, 2009
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patientsM Thys, I Schrauwen, K Vanderstraeten, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
International Journal of Pediatric Otorhinolaryngology|December 22, 1999
Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findingsR F Mueller, A Nehammer, A Middleton, et al.
Genomics|February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, et al.
Pageof 22