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B Wieringa

Showing results (111-120 of 173) with videos related to

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Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
Mechanisms of Development|October 24, 1998
Developmental expression of the cell adhesion molecule-like protein tyrosine phosphatases LAR, RPTPdelta and RPTPsigma in the mouseR Q Schaapveld, J T Schepens, D Bächner, et al.
American Journal of Human Genetics|April 1, 1994
Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in spermG Jansen, P Willems, M Coerwinkel, et al.
Human Genetics|December 1, 1989
Physical fine-mapping of a deletion spanning the Norrie geneP J Diergaarde, B Wieringa, E M Bleeker-Wagemakers, et al.
Human Molecular Genetics|August 1, 1993
No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesG Jansen, M Bartolomei, V Kalscheuer, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Lancet (London, England)|July 25, 1992
Prenatal diagnosis of myotonic dystrophy by direct mutation analysisH J Smeets, W M Nillesen, F Los, et al.
Progress in Clinical and Biological Research|January 1, 1989
Definition of subchromosomal intervals around the myotonic dystrophy locus at 19qH Brunner, M Coerwinkel-Driessen, B Smeets, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12-->q13P M Deen, D O Weghuis, R J Sinke, et al.
The Biochemical Journal|October 15, 1995
Co-localization and functional coupling of creatine kinase B and gastric H+/K(+)-ATPase on the apical membrane and the tubulovesicular system of parietal cellsE A Sistermans, C H Klaassen, W Peters, et al.
Pageof 18

Showing results (111-120 of 173) with videos related to

Sort By:
Pageof 18
Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
Mechanisms of Development|October 24, 1998
Developmental expression of the cell adhesion molecule-like protein tyrosine phosphatases LAR, RPTPdelta and RPTPsigma in the mouseR Q Schaapveld, J T Schepens, D Bächner, et al.
American Journal of Human Genetics|April 1, 1994
Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in spermG Jansen, P Willems, M Coerwinkel, et al.
Human Genetics|December 1, 1989
Physical fine-mapping of a deletion spanning the Norrie geneP J Diergaarde, B Wieringa, E M Bleeker-Wagemakers, et al.
Human Molecular Genetics|August 1, 1993
No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissuesG Jansen, M Bartolomei, V Kalscheuer, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Lancet (London, England)|July 25, 1992
Prenatal diagnosis of myotonic dystrophy by direct mutation analysisH J Smeets, W M Nillesen, F Los, et al.
Progress in Clinical and Biological Research|January 1, 1989
Definition of subchromosomal intervals around the myotonic dystrophy locus at 19qH Brunner, M Coerwinkel-Driessen, B Smeets, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12-->q13P M Deen, D O Weghuis, R J Sinke, et al.
The Biochemical Journal|October 15, 1995
Co-localization and functional coupling of creatine kinase B and gastric H+/K(+)-ATPase on the apical membrane and the tubulovesicular system of parietal cellsE A Sistermans, C H Klaassen, W Peters, et al.
Pageof 18