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G van Camp

Showing results (151-160 of 214) with videos related to

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International Journal of Pediatric Otorhinolaryngology|December 16, 1998
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndromeC W Cremers, R J Admiraal, P L Huygen, 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.
International Journal of Cardiology|September 4, 2020
Heart failure with preserved ejection fraction or non-cardiac dyspnea in paroxysmal atrial fibrillation: The role of left atrial strainA Katbeh, T De Potter, P Geelen, 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.
European Journal of Human Genetics : EJHG|July 1, 1997
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung diseaseC Bidaud, R Salomon, G Van Camp, et al.
Human Mutation|August 19, 2006
KCNQ4: a gene for age-related hearing impairment?E Van Eyken, L Van Laer, E Fransen, et al.
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.
Journal of Medical Genetics|July 1, 1995
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13qG Van Camp, M N Van Thienen, I Handig, et al.
Behavioural Brain Research|March 8, 2011
Impact of early life stress on alcohol consumption and on the short- and long-term responses to alcohol in adolescent female ratsV Van Waes, M Darnaudéry, J Marrocco, et al.
Pageof 22

Showing results (151-160 of 214) with videos related to

Sort By:
Pageof 22
International Journal of Pediatric Otorhinolaryngology|December 16, 1998
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndromeC W Cremers, R J Admiraal, P L Huygen, 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.
International Journal of Cardiology|September 4, 2020
Heart failure with preserved ejection fraction or non-cardiac dyspnea in paroxysmal atrial fibrillation: The role of left atrial strainA Katbeh, T De Potter, P Geelen, 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.
European Journal of Human Genetics : EJHG|July 1, 1997
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung diseaseC Bidaud, R Salomon, G Van Camp, et al.
Human Mutation|August 19, 2006
KCNQ4: a gene for age-related hearing impairment?E Van Eyken, L Van Laer, E Fransen, et al.
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.
Journal of Medical Genetics|July 1, 1995
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13qG Van Camp, M N Van Thienen, I Handig, et al.
Behavioural Brain Research|March 8, 2011
Impact of early life stress on alcohol consumption and on the short- and long-term responses to alcohol in adolescent female ratsV Van Waes, M Darnaudéry, J Marrocco, et al.
Pageof 22