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W Van Hul

Showing results (21-30 of 89) with videos related to

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Calcified Tissue International|May 4, 2013
Localization of the gene for hyperostosis cranialis interna to chromosome 8p21 with analysis of three candidate genesV M Borra, J J Waterval, R J Stokroos, et al.
American Journal of Human Genetics|July 27, 2001
Mapping of autosomal dominant osteopetrosis type II (Albers-Schönberg disease) to chromosome 16p13.3O Bénichou, E Cleiren, J Gram, et al.
Clinical Genetics|October 19, 2010
Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosisB Perdu, P Lakeman, G Mortier, et al.
European Journal of Radiology|December 4, 2001
Hereditary multiple exostoses: from genetics to clinical syndrome and complicationsF M Vanhoenacker, W Van Hul, W Wuyts, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 17, 2005
Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan familyS Simsek, K Janssens, M L Kwee, et al.
Bone|December 12, 2013
Sclerosing bone dysplasias with involvement of the craniofacial skeletonJ J Waterval, V M Borra, W Van Hul, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell linesD Mathysen, N Van Roy, W Van Hul, et al.
Bone|October 23, 2013
Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3-XqterV M Borra, E Steenackers, F de Freitas, et al.
Calcified Tissue International|March 5, 2009
Refined genomic localization of the genetic lesion in the osteopetrosis (op) rat and exclusion of three positional and functional candidate genes, Clcn7, Atp6v0c, and Slc9a3r2B Perdu, P R Odgren, L Van Wesenbeeck, et al.
Molecular Genetics and Metabolism|December 23, 2011
Genetic association between WNT10B polymorphisms and obesity in a Belgian case-control population is restricted to malesJ K Van Camp, S Beckers, D Zegers, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Calcified Tissue International|May 4, 2013
Localization of the gene for hyperostosis cranialis interna to chromosome 8p21 with analysis of three candidate genesV M Borra, J J Waterval, R J Stokroos, et al.
American Journal of Human Genetics|July 27, 2001
Mapping of autosomal dominant osteopetrosis type II (Albers-Schönberg disease) to chromosome 16p13.3O Bénichou, E Cleiren, J Gram, et al.
Clinical Genetics|October 19, 2010
Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosisB Perdu, P Lakeman, G Mortier, et al.
European Journal of Radiology|December 4, 2001
Hereditary multiple exostoses: from genetics to clinical syndrome and complicationsF M Vanhoenacker, W Van Hul, W Wuyts, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 17, 2005
Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan familyS Simsek, K Janssens, M L Kwee, et al.
Bone|December 12, 2013
Sclerosing bone dysplasias with involvement of the craniofacial skeletonJ J Waterval, V M Borra, W Van Hul, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell linesD Mathysen, N Van Roy, W Van Hul, et al.
Bone|October 23, 2013
Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3-XqterV M Borra, E Steenackers, F de Freitas, et al.
Calcified Tissue International|March 5, 2009
Refined genomic localization of the genetic lesion in the osteopetrosis (op) rat and exclusion of three positional and functional candidate genes, Clcn7, Atp6v0c, and Slc9a3r2B Perdu, P R Odgren, L Van Wesenbeeck, et al.
Molecular Genetics and Metabolism|December 23, 2011
Genetic association between WNT10B polymorphisms and obesity in a Belgian case-control population is restricted to malesJ K Van Camp, S Beckers, D Zegers, et al.
Pageof 9