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Bert B A de Vries

Showing results (1-10 of 219) with videos related to

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The Journal of Molecular Diagnostics : JMD|October 27, 2006
Diagnostic genome profiling: unbiased whole genome or targeted analysis?Joris A Veltman, Bert B A de Vries
The Journal of Molecular Diagnostics : JMD|March 27, 2007
Whole-genome array comparative genome hybridization: the preferred diagnostic choice in postnatal clinical cytogeneticsJoris A Veltman, Bert B A de Vries
American Journal of Medical Genetics. Part A|April 12, 2005
Facial characteristics are not distinctive features for the acrofacial dysostosis syndrome type Kennedy-TeebiMariken Ruiter, Pim J van Dijken, Bert B A de Vries
Clinical Dysmorphology|April 2, 2004
Mosaic trisomy 22 in a boy with a terminal transverse limb reduction defectE Mariken Ruiter, Jan Toorman, Ron Hochstenbach, et al.
Clinical Dysmorphology|July 31, 2010
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndromeMariken Ruiter, Erik-Jan Kamsteeg, Germana Meroni, et al.
American Journal of Medical Genetics|April 27, 2002
No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndromeBert B A de Vries, Jess Tyson, Robin M Winter, et al.
Brain Sciences|February 25, 2023
The Genetics of Intellectual DisabilitySandra Jansen, Lisenka E L M Vissers, Bert B A de Vries
European Journal of Human Genetics : EJHG|June 15, 2007
Homozygosity for a FBN1 missense mutation: clinical and molecular evidence for recessive Marfan syndromeBert B A de Vries, Gerard Pals, Roelof Odink, et al.
Journal of Medical Genetics|December 3, 2009
Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosisLisenka E L M Vissers, Bert B A de Vries, Joris A Veltman
Clinical Dysmorphology|February 27, 2015
Vitiligo in the Koolen-de Vries or 17q21.31 microdeletion syndromeAlexander M Maley, Mary K Spraker, Bert B A de Vries, et al.
Pageof 22

Showing results (1-10 of 219) with videos related to

Sort By:
Pageof 22
The Journal of Molecular Diagnostics : JMD|October 27, 2006
Diagnostic genome profiling: unbiased whole genome or targeted analysis?Joris A Veltman, Bert B A de Vries
The Journal of Molecular Diagnostics : JMD|March 27, 2007
Whole-genome array comparative genome hybridization: the preferred diagnostic choice in postnatal clinical cytogeneticsJoris A Veltman, Bert B A de Vries
American Journal of Medical Genetics. Part A|April 12, 2005
Facial characteristics are not distinctive features for the acrofacial dysostosis syndrome type Kennedy-TeebiMariken Ruiter, Pim J van Dijken, Bert B A de Vries
Clinical Dysmorphology|April 2, 2004
Mosaic trisomy 22 in a boy with a terminal transverse limb reduction defectE Mariken Ruiter, Jan Toorman, Ron Hochstenbach, et al.
Clinical Dysmorphology|July 31, 2010
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndromeMariken Ruiter, Erik-Jan Kamsteeg, Germana Meroni, et al.
American Journal of Medical Genetics|April 27, 2002
No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndromeBert B A de Vries, Jess Tyson, Robin M Winter, et al.
Brain Sciences|February 25, 2023
The Genetics of Intellectual DisabilitySandra Jansen, Lisenka E L M Vissers, Bert B A de Vries
European Journal of Human Genetics : EJHG|June 15, 2007
Homozygosity for a FBN1 missense mutation: clinical and molecular evidence for recessive Marfan syndromeBert B A de Vries, Gerard Pals, Roelof Odink, et al.
Journal of Medical Genetics|December 3, 2009
Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosisLisenka E L M Vissers, Bert B A de Vries, Joris A Veltman
Clinical Dysmorphology|February 27, 2015
Vitiligo in the Koolen-de Vries or 17q21.31 microdeletion syndromeAlexander M Maley, Mary K Spraker, Bert B A de Vries, et al.
Pageof 22