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B A van Oost

Showing results (61-70 of 107) with videos related to

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Nature Genetics|October 1, 1992
Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidusA M van den Ouweland, J C Dreesen, M Verdijk, et al.
Science (New York, N.Y.)|April 1, 1994
Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urineP M Deen, M A Verdijk, N V Knoers, et al.
American Journal of Human Genetics|April 1, 1996
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystoniaD D De Vries, L N Went, G W Bruyn, et al.
American Journal of Human Genetics|April 1, 1992
Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2J C Oosterwijk, M Nelen, P M van Zandvoort, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 20, 2000
Refined genetic and comparative physical mapping of the canine copper toxicosis locusB van de Sluis, S Kole, M van Wolferen, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1992
Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch familyJ C Oosterwijk, M Nelen, P M Van Zandvoort, et al.
Cytogenetic and Genome Research|August 17, 2005
The canine sarcoglycan delta gene: BAC clone contig assembly, chromosome assignment and interrogation as a candidate gene for dilated cardiomyopathy in Dobermann dogsP Stabej, P A J Leegwater, S Imholz, et al.
Human Genetics|March 1, 1993
DXS539, a polymorphic DNA marker proximal of the fragile-X geneJ C Dreesen, J A van den Hurk, A P Smits, et al.
American Journal of Medical Genetics|February 1, 1991
Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.
Annals of Neurology|January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndromeI F De Coo, W O Renier, W Ruitenbeek, et al.
Pageof 11

Showing results (61-70 of 107) with videos related to

Sort By:
Pageof 11
Nature Genetics|October 1, 1992
Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidusA M van den Ouweland, J C Dreesen, M Verdijk, et al.
Science (New York, N.Y.)|April 1, 1994
Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urineP M Deen, M A Verdijk, N V Knoers, et al.
American Journal of Human Genetics|April 1, 1996
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystoniaD D De Vries, L N Went, G W Bruyn, et al.
American Journal of Human Genetics|April 1, 1992
Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2J C Oosterwijk, M Nelen, P M van Zandvoort, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 20, 2000
Refined genetic and comparative physical mapping of the canine copper toxicosis locusB van de Sluis, S Kole, M van Wolferen, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1992
Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch familyJ C Oosterwijk, M Nelen, P M Van Zandvoort, et al.
Cytogenetic and Genome Research|August 17, 2005
The canine sarcoglycan delta gene: BAC clone contig assembly, chromosome assignment and interrogation as a candidate gene for dilated cardiomyopathy in Dobermann dogsP Stabej, P A J Leegwater, S Imholz, et al.
Human Genetics|March 1, 1993
DXS539, a polymorphic DNA marker proximal of the fragile-X geneJ C Dreesen, J A van den Hurk, A P Smits, et al.
American Journal of Medical Genetics|February 1, 1991
Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.
Annals of Neurology|January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndromeI F De Coo, W O Renier, W Ruitenbeek, et al.
Pageof 11