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Marijke Bauters

Showing results (1-10 of 23) with videos related to

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Journal of Cellular and Molecular Medicine|November 28, 2006
X-linked mental retardation and epigeneticsGuy Froyen, Marijke Bauters, Thierry Voet, et al.
European Journal of Medical Genetics|September 24, 2005
X chromosome array-CGH for the identification of novel X-linked mental retardation genesMarijke Bauters, Hilde Van Esch, Peter Marynen, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genesHilde Van Esch, Anna Jansen, Marijke Bauters, et al.
British Medical Bulletin|February 12, 2020
Challenges in molecular diagnosis of X-linked Intellectual disabilityChiara De Luca, Valérie Race, Liesbeth Keldermans, et al.
European Journal of Medical Genetics|August 8, 2020
Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactylyMio Aerden, Marijke Bauters, Kris Van Den Bogaert, et al.
FEBS Letters|October 16, 2007
ZIC1 gene expression is controlled by DNA and histone methylation in mesenchymal proliferationsRasoul Pourebrahim, Kim Van Dam, Marijke Bauters, et al.
European Journal of Medical Genetics|April 11, 2015
Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic featuresNathalie Fieremans, Hilde Van Esch, Thomy de Ravel, et al.
American Journal of Medical Genetics. Part A|February 10, 2012
Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1Jeroen Breckpot, Bernard Thienpont, Marijke Bauters, et al.
Human Genetics|July 20, 2014
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivationNathalie Fieremans, Marijke Bauters, Stefanie Belet, et al.
European Journal of Medical Genetics|November 10, 2011
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndromeJeroen Breckpot, Léon-Charles Tranchevent, Bernard Thienpont, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Journal of Cellular and Molecular Medicine|November 28, 2006
X-linked mental retardation and epigeneticsGuy Froyen, Marijke Bauters, Thierry Voet, et al.
European Journal of Medical Genetics|September 24, 2005
X chromosome array-CGH for the identification of novel X-linked mental retardation genesMarijke Bauters, Hilde Van Esch, Peter Marynen, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genesHilde Van Esch, Anna Jansen, Marijke Bauters, et al.
British Medical Bulletin|February 12, 2020
Challenges in molecular diagnosis of X-linked Intellectual disabilityChiara De Luca, Valérie Race, Liesbeth Keldermans, et al.
European Journal of Medical Genetics|August 8, 2020
Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactylyMio Aerden, Marijke Bauters, Kris Van Den Bogaert, et al.
FEBS Letters|October 16, 2007
ZIC1 gene expression is controlled by DNA and histone methylation in mesenchymal proliferationsRasoul Pourebrahim, Kim Van Dam, Marijke Bauters, et al.
European Journal of Medical Genetics|April 11, 2015
Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic featuresNathalie Fieremans, Hilde Van Esch, Thomy de Ravel, et al.
American Journal of Medical Genetics. Part A|February 10, 2012
Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1Jeroen Breckpot, Bernard Thienpont, Marijke Bauters, et al.
Human Genetics|July 20, 2014
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivationNathalie Fieremans, Marijke Bauters, Stefanie Belet, et al.
European Journal of Medical Genetics|November 10, 2011
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndromeJeroen Breckpot, Léon-Charles Tranchevent, Bernard Thienpont, et al.
Pageof 3