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B A van Oost

Showing results (101-110 of 107) with videos related to

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Human Molecular Genetics|August 1, 1994
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndromeH H Lemmink, T Mochizuki, L P van den Heuvel, et al.
American Journal of Human Genetics|October 1, 1994
Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel geneA F van Lieburg, M A Verdijk, V V Knoers, et al.
Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.
Human Molecular Genetics|February 9, 1999
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16B J van de Sluis, M Breen, M Nanji, et al.
Behavior Genetics|December 11, 2007
Evaluation of the serotonergic genes htr1A, htr1B, htr2A, and slc6A4 in aggressive behavior of golden retriever dogsL van den Berg, M Vos-Loohuis, M B H Schilder, et al.
Animal Genetics|November 19, 2005
Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriersO P Forman, M E G Boursnell, B J Dunmore, et al.
Genes, Brain, and Behavior|August 30, 2008
High-resolution genetic mapping of mammalian motor activity levels in miceM J H Kas, J G de Mooij-van Malsen, M de Krom, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 107 results.
Human Molecular Genetics|August 1, 1994
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndromeH H Lemmink, T Mochizuki, L P van den Heuvel, et al.
American Journal of Human Genetics|October 1, 1994
Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel geneA F van Lieburg, M A Verdijk, V V Knoers, et al.
Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.
Human Molecular Genetics|February 9, 1999
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16B J van de Sluis, M Breen, M Nanji, et al.
Behavior Genetics|December 11, 2007
Evaluation of the serotonergic genes htr1A, htr1B, htr2A, and slc6A4 in aggressive behavior of golden retriever dogsL van den Berg, M Vos-Loohuis, M B H Schilder, et al.
Animal Genetics|November 19, 2005
Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriersO P Forman, M E G Boursnell, B J Dunmore, et al.
Genes, Brain, and Behavior|August 30, 2008
High-resolution genetic mapping of mammalian motor activity levels in miceM J H Kas, J G de Mooij-van Malsen, M de Krom, et al.
Pageof 11