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Epigenetics|September 27, 2012
SWI/SNF complex in disorder: SWItching from malignancies to intellectual disabilityGijs W E Santen, Marjolein Kriek, Haico van AttikumGenes|December 9, 2020
Technologies for Pharmacogenomics: A ReviewMaaike van der Lee, Marjolein Kriek, Henk-Jan Guchelaar, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2022
The patient with 41 reports: Analysis of laboratory exome sequencing reporting of a "virtual patient"Danya F Vears, Martin Elferink, Marjolein Kriek, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 30, 2020
Analysis of laboratory reporting practices using a quality assessment of a virtual patientDanya F Vears, Martin Elferink, Marjolein Kriek, et al.European Journal of Human Genetics : EJHG|January 5, 2006
Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplicationsMarjolein Kriek, Stefan J White, Karoly Szuhai, et al.Human Mutation|June 29, 2004
Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostosesStefan J White, Geraldine R Vink, Marjolein Kriek, et al.Human Genetics|June 29, 2007
Refinement of the genetic cause of ATR-16Cornelis L Harteveld, Marjolein Kriek, Emilia K Bijlsma, et al.American Journal of Human Genetics|August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseSaskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.Human Mutation|March 17, 2015
Next-generation diagnostics: gene panel, exome, or whole genome?Yu Sun, Claudia A L Ruivenkamp, Mariëtte J V Hoffer, et al.American Journal of Human Genetics|July 12, 2002
Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridizationStefan White, Margot Kalf, Qiang Liu, et al.Pageof 5