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Patient Education and Counseling|January 13, 2006
Communication with patients during the prenatal testing procedure: an explorative qualitative studyMyra van Zwieten, Dick Willems, Lia Knegt, et al.American Journal of Medical Genetics. Part A|November 26, 2015
Complete and partial XYLT1 deletion in a patient with neonatal short limb skeletal dysplasiaSilvana van Koningsbruggen, Hennie Knoester, Roel Bakx, et al.American Journal of Medical Genetics. Part A|November 12, 2015
Congenital thrombocytopenia in a neonate with an interstitial microdeletion of 3q26.2q26.31Arjan Bouman, Lia Knegt, Stefan Gröschel, et al.Nederlands Tijdschrift Voor Geneeskunde|April 23, 2015
[Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome]Saskia Tamminga, Susanne E Stalman, Gerdine A Kamp, et al.American Journal of Medical Genetics. Part A|January 21, 2016
Trisomy 4 mosaicism: Delineation of the phenotypeArjan Bouman, Anne-Marie van der Kevie-Kersemaekers, Karin Huijsdens-van Amsterdam, et al.Plos One|March 31, 2018
Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonatesPeter Henneman, Arjan Bouman, Adri Mul, et al.Genes & Development|March 21, 2018
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethalityChristina M Ferrer, Marielle Alders, Alex V Postma, et al.Pageof 1