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M Kriek

Showing results (1-10 of 10) with videos related to

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Lancet (London, England)|August 9, 2003
Decreased mortality of ischaemic heart disease among carriers of haemophiliaA Srámek, M Kriek, F R Rosendaal
Lab on a Chip|April 25, 2022
A modular microfluidic platform to enable complex and customisable <i>in vitro</i> models for neuroscienceD Megarity, R Vroman, M Kriek, et al.
European Journal of Medical Genetics|October 24, 2006
Tall stature and duplication of the insulin-like growth factor I receptor geneS G Kant, M Kriek, M J E Walenkamp, et al.
Cytogenetic and Genome Research|March 17, 2009
Methods to detect CNVs in the human genomeE Aten, S J White, M E Kalf, et al.
AJNR. American Journal of Neuroradiology|March 23, 2006
Cerebral white matter abnormalities in 6p25 deletion syndromeM S van der Knaap, M Kriek, W C G Overweg-Plandsoen, et al.
Journal of Medical Genetics|April 3, 2004
Genomic imbalances in mental retardationM Kriek, S J White, M C Bouma, et al.
Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.
Neurogenetics|July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new casesI M de Lange, P Rump, R F Neuteboom, et al.
Clinical Pharmacology and Therapeutics|December 28, 2016
Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics ConsortiumC H van der Wouden, A Cambon-Thomsen, E Cecchin, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Lancet (London, England)|August 9, 2003
Decreased mortality of ischaemic heart disease among carriers of haemophiliaA Srámek, M Kriek, F R Rosendaal
Lab on a Chip|April 25, 2022
A modular microfluidic platform to enable complex and customisable <i>in vitro</i> models for neuroscienceD Megarity, R Vroman, M Kriek, et al.
European Journal of Medical Genetics|October 24, 2006
Tall stature and duplication of the insulin-like growth factor I receptor geneS G Kant, M Kriek, M J E Walenkamp, et al.
Cytogenetic and Genome Research|March 17, 2009
Methods to detect CNVs in the human genomeE Aten, S J White, M E Kalf, et al.
AJNR. American Journal of Neuroradiology|March 23, 2006
Cerebral white matter abnormalities in 6p25 deletion syndromeM S van der Knaap, M Kriek, W C G Overweg-Plandsoen, et al.
Journal of Medical Genetics|April 3, 2004
Genomic imbalances in mental retardationM Kriek, S J White, M C Bouma, et al.
Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.
Neurogenetics|July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new casesI M de Lange, P Rump, R F Neuteboom, et al.
Clinical Pharmacology and Therapeutics|December 28, 2016
Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics ConsortiumC H van der Wouden, A Cambon-Thomsen, E Cecchin, et al.
European Journal of Medical Genetics|April 24, 2012
Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardationE K Bijlsma, A Collins, F T Papa, et al.
Pageof 1