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P Van Hauwe

Showing results (1-10 of 18) with videos related to

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British Journal of Audiology|July 13, 2000
The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner earP Van Hauwe, P Coucke, G Van Camp
American Journal of Medical Genetics|August 5, 2000
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore regionP Van Hauwe, P J Coucke, R J Ensink, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|April 28, 2000
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 regionR J Ensink, P L Huygen, P Van Hauwe, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA 2, 5, 8, 12G Van Camp, P J Coucke, P Van Hauwe, et al.
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.
Genomics|November 5, 1997
Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11K Kastury, W E Taylor, M Gutierrez, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 30, 1998
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndromeW R Cremers, C Bolder, R J Admiraal, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain geneK Kastury, W E Taylor, R Shen, et al.
Microbiology (Reading, England)|November 1, 1996
RP4::Mu3A-mediated in vivo cloning and transfer of a chlorobiphenyl catabolic pathwayD Springael, J van Thor, H Goorissen, 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 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
British Journal of Audiology|July 13, 2000
The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner earP Van Hauwe, P Coucke, G Van Camp
American Journal of Medical Genetics|August 5, 2000
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore regionP Van Hauwe, P J Coucke, R J Ensink, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|April 28, 2000
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 regionR J Ensink, P L Huygen, P Van Hauwe, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA 2, 5, 8, 12G Van Camp, P J Coucke, P Van Hauwe, et al.
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.
Genomics|November 5, 1997
Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11K Kastury, W E Taylor, M Gutierrez, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 30, 1998
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndromeW R Cremers, C Bolder, R J Admiraal, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain geneK Kastury, W E Taylor, R Shen, et al.
Microbiology (Reading, England)|November 1, 1996
RP4::Mu3A-mediated in vivo cloning and transfer of a chlorobiphenyl catabolic pathwayD Springael, J van Thor, H Goorissen, 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 2