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W Van Hul

Showing results (81-90 of 89) with videos related to

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Journal of Medical Genetics|May 17, 2005
Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatmentK Janssens, F Vanhoenacker, M Bonduelle, et al.
International Journal of Obesity (2005)|October 8, 2013
Mutation screen of the SIM1 gene in pediatric patients with early-onset obesityD Zegers, S Beckers, R Hendrickx, 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|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, 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.
Nature Genetics|September 2, 1999
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasiaJ R Hurvitz, W M Suwairi, W Van Hul, 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.
Cell|November 24, 2001
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye developmentY Gong, R B Slee, N Fukai, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Journal of Medical Genetics|May 17, 2005
Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatmentK Janssens, F Vanhoenacker, M Bonduelle, et al.
International Journal of Obesity (2005)|October 8, 2013
Mutation screen of the SIM1 gene in pediatric patients with early-onset obesityD Zegers, S Beckers, R Hendrickx, 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|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, 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.
Nature Genetics|September 2, 1999
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasiaJ R Hurvitz, W M Suwairi, W Van Hul, 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.
Cell|November 24, 2001
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye developmentY Gong, R B Slee, N Fukai, et al.
Pageof 9