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W Van Hul

Showing results (31-40 of 89) with videos related to

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Human Genetics|June 1, 1991
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniquesW Van Hul, H Backhovens, G Van Camp, et al.
Bone|June 1, 2000
Familial Paget's disease of bone: patterns of inheritance and frequency of linkage to chromosome 18qL Hocking, F Slee, S I Haslam, et al.
Human Genetics|October 1, 1991
Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndromeG Van Camp, H Backhovens, M Cruts, et al.
Endocrine|November 30, 2013
Common genetic variation in sFRP5 is associated with fat distribution in menJ K Van Camp, S Beckers, D Zegers, et al.
Genomics|May 1, 1990
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF islandP Stinissen, W Van Hul, G Van Camp, et al.
Human Genetics|August 1, 1989
Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndromeG Van Camp, P Stinissen, W Van Hul, et al.
Acta Radiologica (Stockholm, Sweden : 1987)|July 9, 2003
Camurati-Engelmann disease. Review of radioclinical featuresF M Vanhoenacker, K Janssens, W Van Hul, et al.
Journal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
Clinical Genetics|September 5, 2001
Lack of mutations in the RANK gene in Spanish patients with Paget disease of boneM Marco-Mingot, J L San-Millán, W Wuyts, et al.
American Journal of Human Genetics|August 1, 1997
Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21W Van Hul, J Bollerslev, J Gram, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Human Genetics|June 1, 1991
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniquesW Van Hul, H Backhovens, G Van Camp, et al.
Bone|June 1, 2000
Familial Paget's disease of bone: patterns of inheritance and frequency of linkage to chromosome 18qL Hocking, F Slee, S I Haslam, et al.
Human Genetics|October 1, 1991
Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndromeG Van Camp, H Backhovens, M Cruts, et al.
Endocrine|November 30, 2013
Common genetic variation in sFRP5 is associated with fat distribution in menJ K Van Camp, S Beckers, D Zegers, et al.
Genomics|May 1, 1990
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF islandP Stinissen, W Van Hul, G Van Camp, et al.
Human Genetics|August 1, 1989
Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndromeG Van Camp, P Stinissen, W Van Hul, et al.
Acta Radiologica (Stockholm, Sweden : 1987)|July 9, 2003
Camurati-Engelmann disease. Review of radioclinical featuresF M Vanhoenacker, K Janssens, W Van Hul, et al.
Journal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
Clinical Genetics|September 5, 2001
Lack of mutations in the RANK gene in Spanish patients with Paget disease of boneM Marco-Mingot, J L San-Millán, W Wuyts, et al.
American Journal of Human Genetics|August 1, 1997
Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21W Van Hul, J Bollerslev, J Gram, et al.
Pageof 9