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P Van Hauwe

Showing results (11-20 of 18) with videos related to

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American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.
Nature Genetics|March 18, 1999
Deafness linked to DFNA2: one locus but how many genes?P Van Hauwe, P J Coucke, F Declau, et al.
Journal of Medical Genetics|June 30, 2000
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndromeP J Coucke, P Van Hauwe, L A Everett, et al.
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.
Nature Genetics|March 18, 1999
Deafness linked to DFNA2: one locus but how many genes?P Van Hauwe, P J Coucke, F Declau, et al.
Journal of Medical Genetics|June 30, 2000
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndromeP J Coucke, P Van Hauwe, L A Everett, et al.
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Pageof 2