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Human Mutation|May 16, 2013
0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practiceMalgorzata I Srebniak, Lisanne Mout, Diane Van Opstal, et al.Journal of Medical Ethics|April 12, 2020
Why NIPT should be publicly fundedEline Maria Bunnik, Adriana Kater-Kuipers, Robert-Jan H Galjaard, et al.Journal of Medical Ethics|April 27, 2018
Ethics of routine: a critical analysis of the concept of 'routinisation' in prenatal screeningAdriana Kater-Kuipers, Inez D de Beaufort, Robert-Jan H Galjaard, et al.Bioethics|July 5, 2020
Rethinking counselling in prenatal screening: An ethical analysis of informed consent in the context of non-invasive prenatal testing (NIPT)Adriana Kater-Kuipers, Inez D de Beaufort, Robert-Jan H Galjaard, et al.Journal of Medical Ethics|September 19, 2019
Should pregnant women be charged for non-invasive prenatal screening? Implications for reproductive autonomy and equal accessEline M Bunnik, Adriana Kater-Kuipers, Robert-Jan H Galjaard, et al.Prenatal Diagnosis|May 25, 2023
Non-invasive prenatal testing (NIPT) in twin pregnancies affected by early single fetal demise: A systematic review of NIPT and vanishing twinsJacintha C A van Eekhout, Mireille N Bekker, Caroline J Bax, et al.Molecular Cytogenetics|January 18, 2011
Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosisDiane Van Opstal, Marjan Boter, Petra Noomen, et al.Prenatal Diagnosis|September 10, 2021
Non-invasive prenatal test uptake in socioeconomically disadvantaged neighborhoodsKaruna R M van der Meij, Caroline Kooij, Mireille N Bekker, et al.European Journal of Human Genetics : EJHG|June 23, 2011
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flowMalgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, et al.Journal of Medical Genetics|March 18, 2020
Variable expression of subclinical phenotypes instead of reduced penetrance in families with mild triphalangeal thumb phenotypesJacob W P Potuijt, Jeannette Hoogeboom, Esther de Graaff, et al.Pageof 6