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B A van Oost

Showing results (81-90 of 107) with videos related to

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Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
Human Molecular Genetics|February 1, 1994
Aberrant splicing of the COL4A5 gene in patients with Alport syndromeH H Lemmink, L A Kluijtmans, H G Brunner, et al.
The Journal of Heredity|May 2, 2003
Mapping of rabbit microsatellite markers using chromosome-specific librariesR Korstanje, G F Gillissen, S A Versteeg, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
Biochemical and Biophysical Research Communications|December 14, 2001
Genetic and correlation analysis of hepatic copper content in the ratI D de Wolf, X M Fielmich-Bouman, B A van Oost, et al.
American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.
American Journal of Human Genetics|January 1, 1995
Spectrum of mutations in the gene encoding the adrenoleukodystrophy proteinM J Ligtenberg, S Kemp, C O Sarde, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 3, 2002
Quantitative trait loci influencing hepatic copper in ratsI D de Wolf, A C M Bonné, X M Fielmich-Bouman, et al.
American Journal of Human Genetics|March 1, 1991
Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeG K Suthers, J C Mulley, M A Voelckel, et al.
American Journal of Medical Genetics|April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.
Pageof 11

Showing results (81-90 of 107) with videos related to

Sort By:
Pageof 11
Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
Human Molecular Genetics|February 1, 1994
Aberrant splicing of the COL4A5 gene in patients with Alport syndromeH H Lemmink, L A Kluijtmans, H G Brunner, et al.
The Journal of Heredity|May 2, 2003
Mapping of rabbit microsatellite markers using chromosome-specific librariesR Korstanje, G F Gillissen, S A Versteeg, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
Biochemical and Biophysical Research Communications|December 14, 2001
Genetic and correlation analysis of hepatic copper content in the ratI D de Wolf, X M Fielmich-Bouman, B A van Oost, et al.
American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.
American Journal of Human Genetics|January 1, 1995
Spectrum of mutations in the gene encoding the adrenoleukodystrophy proteinM J Ligtenberg, S Kemp, C O Sarde, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 3, 2002
Quantitative trait loci influencing hepatic copper in ratsI D de Wolf, A C M Bonné, X M Fielmich-Bouman, et al.
American Journal of Human Genetics|March 1, 1991
Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeG K Suthers, J C Mulley, M A Voelckel, et al.
American Journal of Medical Genetics|April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.
Pageof 11