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P Coucke

Showing results (131-140 of 157) with videos related to

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Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.
European Journal of Cancer (Oxford, England : 1990)|December 31, 2002
Shortened irradiation scheme, continuous infusion of 5-fluorouracil and fractionation of mitomycin C in locally advanced anal carcinomas. Results of a phase II study of the European Organization for Research and Treatment of Cancer. Radiotherapy and Gastrointestinal Cooperative GroupsJ F Bosset, F Roelofsen, D A L Morgan, et al.
Revue Medicale De Liege|August 11, 2011
[Hormone therapy for breast cancer]E Lifrange, C Andre, V Bleret, et al.
Human Reproduction (Oxford, England)|March 17, 2023
Assisted oocyte activation does not overcome recurrent embryo developmental problemsA Cardona Barberán, D Bonte, A Boel, et al.
Clinical and Experimental Immunology|April 6, 2005
CARD15 polymorphisms are associated with anti-Saccharomyces cerevisiae antibodies in caucasian Crohn's disease patientsB Vander Cruyssen, H Peeters, I E A Hoffman, 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.
American Journal of Human Genetics|June 12, 1999
A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3K Fukushima, N Kasai, Y Ueki, et al.
American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, 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.
Pageof 16

Showing results (131-140 of 157) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.
European Journal of Cancer (Oxford, England : 1990)|December 31, 2002
Shortened irradiation scheme, continuous infusion of 5-fluorouracil and fractionation of mitomycin C in locally advanced anal carcinomas. Results of a phase II study of the European Organization for Research and Treatment of Cancer. Radiotherapy and Gastrointestinal Cooperative GroupsJ F Bosset, F Roelofsen, D A L Morgan, et al.
Revue Medicale De Liege|August 11, 2011
[Hormone therapy for breast cancer]E Lifrange, C Andre, V Bleret, et al.
Human Reproduction (Oxford, England)|March 17, 2023
Assisted oocyte activation does not overcome recurrent embryo developmental problemsA Cardona Barberán, D Bonte, A Boel, et al.
Clinical and Experimental Immunology|April 6, 2005
CARD15 polymorphisms are associated with anti-Saccharomyces cerevisiae antibodies in caucasian Crohn's disease patientsB Vander Cruyssen, H Peeters, I E A Hoffman, 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.
American Journal of Human Genetics|June 12, 1999
A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3K Fukushima, N Kasai, Y Ueki, et al.
American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, 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.
Pageof 16