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G van Camp

Showing results (121-130 of 214) with videos related to

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The Laryngoscope|January 31, 1998
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2H Kunst, H Marres, P Huygen, et al.
Heart (British Cardiac Society)|October 13, 2010
Impact of prosthesis-patient mismatch on mitral regurgitation after aortic valve replacementP Unger, J Magne, F Vanden Eynden, et al.
Clinical Genetics|May 6, 2011
DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairmentM A Tabatabaiefar, F Alasti, L Shariati, et al.
Genomics|September 21, 2000
Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPESE De Baere, Y Fukushima, K Small, et al.
Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
Oncology|January 1, 1985
Treatment with recombinant interferon-alpha-2C: multiple myeloma and thrombocythaemia in myeloproliferative diseasesH Ludwig, A Cortelezzi, B G Van Camp, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
The Annals of Otology, Rhinology, and Laryngology|March 28, 2002
Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 familyEls M R De Leenheer, Patrick L M Huygen, Paul J Coucke, et al.
Pageof 22

Showing results (121-130 of 214) with videos related to

Sort By:
Pageof 22
The Laryngoscope|January 31, 1998
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2H Kunst, H Marres, P Huygen, et al.
Heart (British Cardiac Society)|October 13, 2010
Impact of prosthesis-patient mismatch on mitral regurgitation after aortic valve replacementP Unger, J Magne, F Vanden Eynden, et al.
Clinical Genetics|May 6, 2011
DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairmentM A Tabatabaiefar, F Alasti, L Shariati, et al.
Genomics|September 21, 2000
Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPESE De Baere, Y Fukushima, K Small, et al.
Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
Oncology|January 1, 1985
Treatment with recombinant interferon-alpha-2C: multiple myeloma and thrombocythaemia in myeloproliferative diseasesH Ludwig, A Cortelezzi, B G Van Camp, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
The Annals of Otology, Rhinology, and Laryngology|March 28, 2002
Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 familyEls M R De Leenheer, Patrick L M Huygen, Paul J Coucke, et al.
Pageof 22