Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B A van Oost

Showing results (41-50 of 107) with videos related to

Pageof 11
Sort By:
Genomics|April 1, 1989
Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidusN Knoers, H van der Heyden, B A van Oost, et al.
American Journal of Medical Genetics|April 1, 1992
Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeB A van Oost, A P Smits, J C Dreesen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutationZ Hochberg, A Van Lieburg, L Even, et al.
Thrombosis and Haemostasis|June 28, 1982
Determination of the density distribution of human platelets--methodological aspects and comparison with other tests for platelet activationB A van Oost, I H van Hien-Hagg, B F Veldhuyzen, et al.
Human Molecular Genetics|July 1, 1992
Identification and characterization of a new gene in the human Xq28 regionA M van den Ouweland, P Kioschis, M Verdijk, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
British Medical Journal (Clinical Research Ed.)|February 20, 1982
Listeria monocytogenes meningitis and decreased phagocytosis associated with iron overloadB S van Asbeck, H A Verbrugh, B A van Oost, et al.
Cytogenetics and Cell Genetics|April 25, 2000
Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogsI S Lantinga-van Leeuwen, H S Kooistra, J A Mol, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 2000
Isolation of DNA markers informative in purebred dog families by genomic representational difference analysis (gRDA)R E Everts, S A Versteeg, C Renier, et al.
Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.
Pageof 11

Showing results (41-50 of 107) with videos related to

Sort By:
Pageof 11
Genomics|April 1, 1989
Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidusN Knoers, H van der Heyden, B A van Oost, et al.
American Journal of Medical Genetics|April 1, 1992
Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeB A van Oost, A P Smits, J C Dreesen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutationZ Hochberg, A Van Lieburg, L Even, et al.
Thrombosis and Haemostasis|June 28, 1982
Determination of the density distribution of human platelets--methodological aspects and comparison with other tests for platelet activationB A van Oost, I H van Hien-Hagg, B F Veldhuyzen, et al.
Human Molecular Genetics|July 1, 1992
Identification and characterization of a new gene in the human Xq28 regionA M van den Ouweland, P Kioschis, M Verdijk, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
British Medical Journal (Clinical Research Ed.)|February 20, 1982
Listeria monocytogenes meningitis and decreased phagocytosis associated with iron overloadB S van Asbeck, H A Verbrugh, B A van Oost, et al.
Cytogenetics and Cell Genetics|April 25, 2000
Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogsI S Lantinga-van Leeuwen, H S Kooistra, J A Mol, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 2000
Isolation of DNA markers informative in purebred dog families by genomic representational difference analysis (gRDA)R E Everts, S A Versteeg, C Renier, et al.
Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.
Pageof 11