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W Van Hul

Showing results (61-70 of 89) with videos related to

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American Journal of Human Genetics|September 1, 1991
DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)E Bakker, C van Broeckhoven, J Haan, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.
Nature Genetics|November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann diseaseK Janssens, R Gershoni-Baruch, N Guañabens, et al.
Bone|February 13, 2001
Evaluation of the role of RANK and OPG genes in Paget's disease of boneW Wuyts, L Van Wesenbeeck, A Morales-Piga, et al.
Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.
American Journal of Human Genetics|April 16, 1998
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21W Van Hul, W Balemans, E Van Hul, et al.
Nature Genetics|June 1, 1992
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein geneL Hendriks, C M van Duijn, P Cras, et al.
Nature|October 8, 1987
Germline mosaicism and Duchenne muscular dystrophy mutationsE Bakker, C Van Broeckhoven, E J Bonten, et al.
American Journal of Human Genetics|September 14, 2001
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35L J Hocking, C A Herbert, R K Nicholls, et al.
Nature Genetics|December 30, 1999
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysisA E Hughes, S H Ralston, J Marken, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|September 1, 1991
DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)E Bakker, C van Broeckhoven, J Haan, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.
Nature Genetics|November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann diseaseK Janssens, R Gershoni-Baruch, N Guañabens, et al.
Bone|February 13, 2001
Evaluation of the role of RANK and OPG genes in Paget's disease of boneW Wuyts, L Van Wesenbeeck, A Morales-Piga, et al.
Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.
American Journal of Human Genetics|April 16, 1998
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21W Van Hul, W Balemans, E Van Hul, et al.
Nature Genetics|June 1, 1992
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein geneL Hendriks, C M van Duijn, P Cras, et al.
Nature|October 8, 1987
Germline mosaicism and Duchenne muscular dystrophy mutationsE Bakker, C Van Broeckhoven, E J Bonten, et al.
American Journal of Human Genetics|September 14, 2001
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35L J Hocking, C A Herbert, R K Nicholls, et al.
Nature Genetics|December 30, 1999
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysisA E Hughes, S H Ralston, J Marken, et al.
Pageof 9