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W Van Hul

Showing results (11-20 of 89) with videos related to

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International Journal of Obesity (2005)|October 19, 2005
Screening for melanocortin-4 receptor mutations in a cohort of Belgian morbidly obese adults and childrenS Beckers, I Mertens, A Peeters, et al.
Human Mutation|September 8, 1999
A novel frameshift mutation (1651ins5) in exon 10 of the CFTR gene can be misinterpreted as a DeltaF508 mutationG Delaere, K Stuer, K Storm, et al.
European Journal of Radiology|December 4, 2001
Congenital skeletal abnormalities: an introduction to the radiological semiologyF M Vanhoenacker, W Van Hul, J Gielen, et al.
American Journal of Medical Genetics|May 9, 2001
Burning down DEFECT11W Wuyts, W Van Hul, O Bartsch, et al.
European Journal of Radiology|December 4, 2001
Molecular and radiological diagnosis of sclerosing bone dysplasiasW Van Hul, F Vanhoenacker, W Balemans, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mappingD Mathysen, W Wuyts, P J Bossuyt, et al.
Bone|March 22, 2005
An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutationK Janssens, M-C de Vernejoul, F de Freitas, et al.
Calcified Tissue International|November 23, 2006
Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American familyG Beyens, W Wuyts, E Cleiren, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 12, 2000
Further evidence for genetic heterogeneity within type II autosomal dominant osteopetrosisO D Bénichou, B Bénichou, H Copin, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
International Journal of Obesity (2005)|October 19, 2005
Screening for melanocortin-4 receptor mutations in a cohort of Belgian morbidly obese adults and childrenS Beckers, I Mertens, A Peeters, et al.
Human Mutation|September 8, 1999
A novel frameshift mutation (1651ins5) in exon 10 of the CFTR gene can be misinterpreted as a DeltaF508 mutationG Delaere, K Stuer, K Storm, et al.
European Journal of Radiology|December 4, 2001
Congenital skeletal abnormalities: an introduction to the radiological semiologyF M Vanhoenacker, W Van Hul, J Gielen, et al.
American Journal of Medical Genetics|May 9, 2001
Burning down DEFECT11W Wuyts, W Van Hul, O Bartsch, et al.
European Journal of Radiology|December 4, 2001
Molecular and radiological diagnosis of sclerosing bone dysplasiasW Van Hul, F Vanhoenacker, W Balemans, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mappingD Mathysen, W Wuyts, P J Bossuyt, et al.
Bone|March 22, 2005
An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutationK Janssens, M-C de Vernejoul, F de Freitas, et al.
Calcified Tissue International|November 23, 2006
Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American familyG Beyens, W Wuyts, E Cleiren, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 12, 2000
Further evidence for genetic heterogeneity within type II autosomal dominant osteopetrosisO D Bénichou, B Bénichou, H Copin, et al.
Pageof 9