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W Balemans

Showing results (11-20 of 19) with videos related to

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Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, 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.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
American Journal of Human Genetics|May 20, 1999
Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21W Balemans, J Van Den Ende, A Freire Paes-Alves, et al.
Journal of Medical Genetics|February 12, 2002
Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem diseaseW Balemans, N Patel, M Ebeling, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Journal of Dental Research|July 10, 2009
Sclerostin in mineralized matrices and van Buchem diseaseR L van Bezooijen, A L Bronckers, R A Gortzak, et al.
Human Molecular Genetics|February 22, 2001
Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)W Balemans, M Ebeling, N Patel, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, 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.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
American Journal of Human Genetics|May 20, 1999
Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21W Balemans, J Van Den Ende, A Freire Paes-Alves, et al.
Journal of Medical Genetics|February 12, 2002
Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem diseaseW Balemans, N Patel, M Ebeling, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Journal of Dental Research|July 10, 2009
Sclerostin in mineralized matrices and van Buchem diseaseR L van Bezooijen, A L Bronckers, R A Gortzak, et al.
Human Molecular Genetics|February 22, 2001
Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)W Balemans, M Ebeling, N Patel, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
Pageof 2