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B A van Oost

Showing results (91-100 of 107) with videos related to

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Genomics|August 1, 1993
Identification of four novel mutations in the COL4A5 gene of patients with Alport syndromeH H Lemmink, C H Schröder, H G Brunner, et al.
Genomics|July 1, 1991
Linkage homogeneity near the fragile X locus in normal and fragile X familiesG K Suthers, J C Mulley, M A Voelckel, et al.
Animal Genetics|December 23, 2003
Development of a single nucleotide polymorphism map of porcine chromosome 2B J Jungerius, A P Rattink, R P M A Crooijmans, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
American Journal of Human Genetics|June 1, 1993
X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolismH G Brunner, M R Nelen, P van Zandvoort, et al.
Biochemical and Biophysical Research Communications|July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutationsS Kemp, M J Ligtenberg, B M van Geel, et al.
American Journal of Human Genetics|January 1, 1996
Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular diseaseL A Kluijtmans, L P van den Heuvel, G H Boers, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Genomics|August 1, 1992
Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 regionA M van den Ouweland, M T Knoop, V V Knoers, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
Genomics|August 1, 1993
Identification of four novel mutations in the COL4A5 gene of patients with Alport syndromeH H Lemmink, C H Schröder, H G Brunner, et al.
Genomics|July 1, 1991
Linkage homogeneity near the fragile X locus in normal and fragile X familiesG K Suthers, J C Mulley, M A Voelckel, et al.
Animal Genetics|December 23, 2003
Development of a single nucleotide polymorphism map of porcine chromosome 2B J Jungerius, A P Rattink, R P M A Crooijmans, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
American Journal of Human Genetics|June 1, 1993
X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolismH G Brunner, M R Nelen, P van Zandvoort, et al.
Biochemical and Biophysical Research Communications|July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutationsS Kemp, M J Ligtenberg, B M van Geel, et al.
American Journal of Human Genetics|January 1, 1996
Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular diseaseL A Kluijtmans, L P van den Heuvel, G H Boers, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Genomics|August 1, 1992
Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 regionA M van den Ouweland, M T Knoop, V V Knoers, et al.
Pageof 11