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M Bleeker

Showing results (31-40 of 103) with videos related to

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The New Phytologist|April 20, 2021
Mechanisms of arsenate tolerance in Cytisus striatusPetra M Bleeker, Henk Schat, Riet Vooijs, et al.
Journal of Medical Genetics|December 1, 1994
Refinement of the chromosomal position of the X linked juvenile retinoschisis geneA A Bergen, J B ten Brink, L M Bleeker-Wagemakers, et al.
American Journal of Medical Genetics|July 24, 1998
Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?U Moog, E M Bleeker-Wagemakers, P Crobach, et al.
European Journal of Pediatrics|July 1, 1990
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive courseP G Barth, R J Wanders, R B Schutgens, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1991
DNA diagnosis in a family with autosomal dominant aniridiaF D Verbraak, M A Mannens, E J Redeker, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Posthumous diagnosis of X-linked retinoschisis using DNA analysisM J van Schooneveld, E M Bleeker-Wagemakers, U Orth, et al.
Blood|January 1, 1992
Localization of the platelet-specific HPA-2 (Ko) alloantigens on the N-terminal globular fragment of platelet glycoprotein Ib alphaR W Kuijpers, W H Ouwehand, P M Bleeker, et al.
Survey of Ophthalmology|February 20, 1999
Retinitis pigmentosa: defined from a molecular point of viewS van Soest, A Westerveld, P T de Jong, et al.
Microbiology (Reading, England)|July 1, 1996
Evaluation of the DNA fingerprinting method AFLP as an new tool in bacterial taxonomyP Janssen, R Coopman, G Huys, et al.
Journal of Medical Genetics|April 1, 1994
Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcomeR J Oostra, P A Bolhuis, F A Wijburg, et al.
Pageof 11

Showing results (31-40 of 103) with videos related to

Sort By:
Pageof 11
The New Phytologist|April 20, 2021
Mechanisms of arsenate tolerance in Cytisus striatusPetra M Bleeker, Henk Schat, Riet Vooijs, et al.
Journal of Medical Genetics|December 1, 1994
Refinement of the chromosomal position of the X linked juvenile retinoschisis geneA A Bergen, J B ten Brink, L M Bleeker-Wagemakers, et al.
American Journal of Medical Genetics|July 24, 1998
Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?U Moog, E M Bleeker-Wagemakers, P Crobach, et al.
European Journal of Pediatrics|July 1, 1990
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive courseP G Barth, R J Wanders, R B Schutgens, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1991
DNA diagnosis in a family with autosomal dominant aniridiaF D Verbraak, M A Mannens, E J Redeker, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Posthumous diagnosis of X-linked retinoschisis using DNA analysisM J van Schooneveld, E M Bleeker-Wagemakers, U Orth, et al.
Blood|January 1, 1992
Localization of the platelet-specific HPA-2 (Ko) alloantigens on the N-terminal globular fragment of platelet glycoprotein Ib alphaR W Kuijpers, W H Ouwehand, P M Bleeker, et al.
Survey of Ophthalmology|February 20, 1999
Retinitis pigmentosa: defined from a molecular point of viewS van Soest, A Westerveld, P T de Jong, et al.
Microbiology (Reading, England)|July 1, 1996
Evaluation of the DNA fingerprinting method AFLP as an new tool in bacterial taxonomyP Janssen, R Coopman, G Huys, et al.
Journal of Medical Genetics|April 1, 1994
Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcomeR J Oostra, P A Bolhuis, F A Wijburg, et al.
Pageof 11