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A van Haeringen

Showing results (31-40 of 60) with videos related to

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Lancet (London, England)|July 27, 1991
Fetal dystrophin to diagnose carrier statusI B Ginjaar, S Soffers, A F Moorman, et al.
Journal of Medical Genetics|October 21, 2005
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experienceZ A Bhuiyan, M Klein, P Hammond, et al.
American Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.
Journal of Medical Genetics|May 1, 1997
Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics WorkgroupA C DudokdeWit, A Tibben, H J Duivenvoorden, et al.
Cytogenetic and Genome Research|May 1, 2010
A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplicationA C J Gijsbers, A van Haeringen, C A J Bosch, et al.
American Journal of Medical Genetics. Part A|August 16, 2005
Bifurcation of the femur with tibial agenesis and additional anomaliesJ M van de Kamp, J J van der Smagt, C F A Bos, et al.
Molecular Biotechnology|March 14, 2003
Detection of universal variable fragments as markers for genetic studies. A novel technology for DNA fingerprintingW A van Haeringen, L H P van de Goor, H Panneman, et al.
Psycho-Oncology|March 4, 2005
Hereditary melanoma and predictive genetic testing: why not?S R Riedijk, F A de Snoo, S van Dijk, et al.
The Journal of Heredity|September 6, 2001
Mapping of a QTL for serum HDL cholesterol in the rabbit using AFLP technologyW A Van Haeringen, M Den Bieman, G F Gillissen, et al.
Journal of Medical Genetics|July 1, 1997
Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3S G Kant, A Van Haeringen, E Bakker, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Lancet (London, England)|July 27, 1991
Fetal dystrophin to diagnose carrier statusI B Ginjaar, S Soffers, A F Moorman, et al.
Journal of Medical Genetics|October 21, 2005
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experienceZ A Bhuiyan, M Klein, P Hammond, et al.
American Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.
Journal of Medical Genetics|May 1, 1997
Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics WorkgroupA C DudokdeWit, A Tibben, H J Duivenvoorden, et al.
Cytogenetic and Genome Research|May 1, 2010
A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplicationA C J Gijsbers, A van Haeringen, C A J Bosch, et al.
American Journal of Medical Genetics. Part A|August 16, 2005
Bifurcation of the femur with tibial agenesis and additional anomaliesJ M van de Kamp, J J van der Smagt, C F A Bos, et al.
Molecular Biotechnology|March 14, 2003
Detection of universal variable fragments as markers for genetic studies. A novel technology for DNA fingerprintingW A van Haeringen, L H P van de Goor, H Panneman, et al.
Psycho-Oncology|March 4, 2005
Hereditary melanoma and predictive genetic testing: why not?S R Riedijk, F A de Snoo, S van Dijk, et al.
The Journal of Heredity|September 6, 2001
Mapping of a QTL for serum HDL cholesterol in the rabbit using AFLP technologyW A Van Haeringen, M Den Bieman, G F Gillissen, et al.
Journal of Medical Genetics|July 1, 1997
Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3S G Kant, A Van Haeringen, E Bakker, et al.
Pageof 6