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W Van Hul

Showing results (41-50 of 89) with videos related to

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Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.
Genomics|February 12, 1998
The human extracellular matrix gene 1 (ECM1): genomic structure, cDNA cloning, expression pattern, and chromosomal localizationP Smits, J Ni, P Feng, et al.
British Journal of Cancer|July 20, 2001
A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosisC Y Xiao, J Wang, S Z Zhang, et al.
Genomics|July 15, 1994
Cloning and characterization of a 135- to 500-kb region of homology on the long arm of human chromosome 21A Dutriaux, J Rossier, W Van Hul, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Molecular and clinical examination of an Italian DEFECT11 familyW Wuyts, G Di Gennaro, F Bianco, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mappingW Van Hul, G Hong, J Wauters, 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.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 27, 2020
Multiple bilateral hip fractures in a patient with dyskeratosis congenita caused by a novel mutation in the PARN geneZ Belaya, O Golounina, A Nikitin, et al.
Genomics|February 28, 1998
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene familyW Van Hul, W Wuyts, J Hendrickx, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.
Genomics|February 12, 1998
The human extracellular matrix gene 1 (ECM1): genomic structure, cDNA cloning, expression pattern, and chromosomal localizationP Smits, J Ni, P Feng, et al.
British Journal of Cancer|July 20, 2001
A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosisC Y Xiao, J Wang, S Z Zhang, et al.
Genomics|July 15, 1994
Cloning and characterization of a 135- to 500-kb region of homology on the long arm of human chromosome 21A Dutriaux, J Rossier, W Van Hul, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Molecular and clinical examination of an Italian DEFECT11 familyW Wuyts, G Di Gennaro, F Bianco, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mappingW Van Hul, G Hong, J Wauters, 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.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 27, 2020
Multiple bilateral hip fractures in a patient with dyskeratosis congenita caused by a novel mutation in the PARN geneZ Belaya, O Golounina, A Nikitin, et al.
Genomics|February 28, 1998
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene familyW Van Hul, W Wuyts, J Hendrickx, et al.
Pageof 9