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M Bleeker

Showing results (81-90 of 103) with videos related to

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Genomics|November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaL M Bleeker-Wagemakers, A Gal, R Kumar-Singh, et al.
The Journal of General Virology|February 1, 1988
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11A de Ronde, M Mannens, R M Slater, et al.
Clinical Genetics|June 1, 1997
On the many faces of Leber hereditary optic neuropathyR J Oostra, N T Tijmes, J M Cobben, et al.
Vox Sanguinis|January 1, 1994
Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphismsS Simsek, C A de Jong, H T Cuijpers, et al.
The British Journal of Ophthalmology|December 1, 1984
Lymphoid proliferations in the orbit: malignant or benign?R van der Gaag, L Koornneef, P van Heerde, et al.
Brain : a Journal of Neurology|April 29, 1998
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonG M Terwindt, J Haan, R A Ophoff, et al.
Drug and Alcohol Review|April 20, 2022
The Overdose Response with Take Home Naloxone (ORTHN) project: Evaluation of health worker training, attitudes and perceptionsLauren A Monds, Maria Bravo, Llewellyn Mills, et al.
Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A sibship with a mild variant of Zellweger syndromeP G Barth, R B Schutgens, R J Wanders, et al.
American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Genomics|November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaL M Bleeker-Wagemakers, A Gal, R Kumar-Singh, et al.
The Journal of General Virology|February 1, 1988
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11A de Ronde, M Mannens, R M Slater, et al.
Clinical Genetics|June 1, 1997
On the many faces of Leber hereditary optic neuropathyR J Oostra, N T Tijmes, J M Cobben, et al.
Vox Sanguinis|January 1, 1994
Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphismsS Simsek, C A de Jong, H T Cuijpers, et al.
The British Journal of Ophthalmology|December 1, 1984
Lymphoid proliferations in the orbit: malignant or benign?R van der Gaag, L Koornneef, P van Heerde, et al.
Brain : a Journal of Neurology|April 29, 1998
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonG M Terwindt, J Haan, R A Ophoff, et al.
Drug and Alcohol Review|April 20, 2022
The Overdose Response with Take Home Naloxone (ORTHN) project: Evaluation of health worker training, attitudes and perceptionsLauren A Monds, Maria Bravo, Llewellyn Mills, et al.
Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A sibship with a mild variant of Zellweger syndromeP G Barth, R B Schutgens, R J Wanders, et al.
American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.
Pageof 11