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W Balemans

Showing results (1-10 of 19) with videos related to

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Journal of Musculoskeletal & Neuronal Interactions|December 24, 2004
Identification of the disease-causing gene in sclerosteosis--discovery of a novel bone anabolic target?W Balemans, W Van Hul
Calcified Tissue International|November 25, 2005
A clinical and molecular overview of the human osteopetrosesW Balemans, L Van Wesenbeeck, W Van Hul
European Journal of Radiology|December 4, 2001
Molecular and radiological diagnosis of sclerosing bone dysplasiasW Van Hul, F Vanhoenacker, W Balemans, et al.
European Neurology|September 4, 1999
Classical Friedreich's ataxia and its genotypeJ Martin, L Martin, A Löfgren, et al.
Bone|October 26, 2002
Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphismsW Balemans, D Foernzler, C Parsons, et al.
European Radiology|September 21, 2000
Sclerosing bone dysplasias: genetic and radioclinical featuresF M Vanhoenacker, L H De Beuckeleer, W Van Hul, et al.
American Journal of Human Genetics|April 16, 1998
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21W Van Hul, W Balemans, E Van Hul, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 17, 1998
Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneityS I Haslam, W Van Hul, A Morales-Piga, et al.
Calcified Tissue International|December 7, 2007
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen studyK Brixen, S Beckers, A Peeters, et al.
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.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Journal of Musculoskeletal & Neuronal Interactions|December 24, 2004
Identification of the disease-causing gene in sclerosteosis--discovery of a novel bone anabolic target?W Balemans, W Van Hul
Calcified Tissue International|November 25, 2005
A clinical and molecular overview of the human osteopetrosesW Balemans, L Van Wesenbeeck, W Van Hul
European Journal of Radiology|December 4, 2001
Molecular and radiological diagnosis of sclerosing bone dysplasiasW Van Hul, F Vanhoenacker, W Balemans, et al.
European Neurology|September 4, 1999
Classical Friedreich's ataxia and its genotypeJ Martin, L Martin, A Löfgren, et al.
Bone|October 26, 2002
Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphismsW Balemans, D Foernzler, C Parsons, et al.
European Radiology|September 21, 2000
Sclerosing bone dysplasias: genetic and radioclinical featuresF M Vanhoenacker, L H De Beuckeleer, W Van Hul, et al.
American Journal of Human Genetics|April 16, 1998
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21W Van Hul, W Balemans, E Van Hul, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 17, 1998
Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneityS I Haslam, W Van Hul, A Morales-Piga, et al.
Calcified Tissue International|December 7, 2007
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen studyK Brixen, S Beckers, A Peeters, et al.
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.
Pageof 2