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W Van Hul

Showing results (51-60 of 89) with videos related to

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European Radiology|September 21, 2000
Sclerosing bone dysplasias: genetic and radioclinical featuresF M Vanhoenacker, L H De Beuckeleer, W Van Hul, et al.
European Journal of Endocrinology|July 1, 2010
Polymorphisms in the endocannabinoid receptor 1 in relation to fat mass distributionM Frost, T L Nielsen, K Wraae, et al.
Cytogenetics and Cell Genetics|November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 geneW Wuyts, N Spieker, N Van Roy, et al.
Genomics|August 1, 1992
D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21A C Warren, M B Petersen, W Van Hul, et al.
Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.
Endocrine|July 7, 2012
No conclusive evidence for association of polymorphisms in the adiponectin receptor 1 gene, AdipoR1, with common obesityS Beckers, F de Freitas, D Zegers, et al.
Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.
Genomics|March 1, 1993
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13EW Van Hul, G Van Camp, L Stuyver, et al.
American Journal of Human Genetics|August 12, 1999
EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomasJ V Bovée, A M Cleton-Jansen, W Wuyts, 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.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
European Radiology|September 21, 2000
Sclerosing bone dysplasias: genetic and radioclinical featuresF M Vanhoenacker, L H De Beuckeleer, W Van Hul, et al.
European Journal of Endocrinology|July 1, 2010
Polymorphisms in the endocannabinoid receptor 1 in relation to fat mass distributionM Frost, T L Nielsen, K Wraae, et al.
Cytogenetics and Cell Genetics|November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 geneW Wuyts, N Spieker, N Van Roy, et al.
Genomics|August 1, 1992
D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21A C Warren, M B Petersen, W Van Hul, et al.
Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.
Endocrine|July 7, 2012
No conclusive evidence for association of polymorphisms in the adiponectin receptor 1 gene, AdipoR1, with common obesityS Beckers, F de Freitas, D Zegers, et al.
Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.
Genomics|March 1, 1993
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13EW Van Hul, G Van Camp, L Stuyver, et al.
American Journal of Human Genetics|August 12, 1999
EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomasJ V Bovée, A M Cleton-Jansen, W Wuyts, 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.
Pageof 9