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G van Camp

Showing results (101-110 of 214) with videos related to

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Journal of Medical Genetics|July 22, 2005
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locusW Chen, K Kahrizi, N C Meyer, et al.
Archives of Otolaryngology--Head & Neck Surgery|June 1, 1997
Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2H Marres, M van Ewijk, P Huygen, et al.
Human Genetics|September 15, 2000
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypesJ Balciuniene, N Dahl, P Jalonen, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13W T McGuirt, M M Lesperance, E R Wilcox, et al.
Brain Research|May 30, 2001
Activities of the pituitary-adrenal and gonadal axes during the estrous cycle in adult female rats prenatally exposed to morphineI Dutriez-Casteloot, V Montel, D Croix, et al.
European Heart Journal|August 1, 1995
Adult onset Kawasaki disease diagnosed by the echocardiographic demonstration of coronary aneurysmsG Van Camp, P Deschamps, F Mestrez, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Frontiers in Genetics|November 25, 2022
Structure and evolution of the squamate major histocompatibility complex as revealed by two <i>Anolis</i> lizard genomesDaren C Card, Andrew G Van Camp, Trenten Santonastaso, et al.
Genomics|November 20, 1995
The gene for human gap junction protein connexin37 (GJA4) maps to chromosome 1p35.1, in the vicinity of D1S195G Van Camp, P Coucke, F Speleman, et al.
HNO|September 5, 2009
[Influence of exogenic factors on age-related hearing impairment]M Baur, E Fransen, A Tropitzsch, et al.
Pageof 22

Showing results (101-110 of 214) with videos related to

Sort By:
Pageof 22
Journal of Medical Genetics|July 22, 2005
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locusW Chen, K Kahrizi, N C Meyer, et al.
Archives of Otolaryngology--Head & Neck Surgery|June 1, 1997
Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2H Marres, M van Ewijk, P Huygen, et al.
Human Genetics|September 15, 2000
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypesJ Balciuniene, N Dahl, P Jalonen, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13W T McGuirt, M M Lesperance, E R Wilcox, et al.
Brain Research|May 30, 2001
Activities of the pituitary-adrenal and gonadal axes during the estrous cycle in adult female rats prenatally exposed to morphineI Dutriez-Casteloot, V Montel, D Croix, et al.
European Heart Journal|August 1, 1995
Adult onset Kawasaki disease diagnosed by the echocardiographic demonstration of coronary aneurysmsG Van Camp, P Deschamps, F Mestrez, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Frontiers in Genetics|November 25, 2022
Structure and evolution of the squamate major histocompatibility complex as revealed by two <i>Anolis</i> lizard genomesDaren C Card, Andrew G Van Camp, Trenten Santonastaso, et al.
Genomics|November 20, 1995
The gene for human gap junction protein connexin37 (GJA4) maps to chromosome 1p35.1, in the vicinity of D1S195G Van Camp, P Coucke, F Speleman, et al.
HNO|September 5, 2009
[Influence of exogenic factors on age-related hearing impairment]M Baur, E Fransen, A Tropitzsch, et al.
Pageof 22