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Nederlands Tijdschrift Voor Geneeskunde|October 25, 2002
[Amyoplasia congenita: a serious congenital abnormality with a relatively favorable prognosis]R Petru, A Verrips, C M A van RavenswaaijCytogenetic and Genome Research|November 25, 2006
Cytogenetic genotype-phenotype studies: improving genotyping, phenotyping and data storageI Feenstra, H G Brunner, C M A van RavenswaaijAJNR. American Journal of Neuroradiology|September 22, 2018
Imaging of Clival Hypoplasia in CHARGE Syndrome and Hypothesis for Development: A Case-Control StudyC M de Geus, J E H Bergman, C M A van Ravenswaaij-Arts, et al.Neuropediatrics|June 15, 2006
Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8I Feenstra, C M A van Ravenswaaij, M S van der Knaap, et al.Human Reproduction (Oxford, England)|September 18, 2010
Who should be screened for chromosomal abnormalities before ICSI treatment?E C Dul, C M A van Ravenswaaij-Arts, H Groen, et al.Human Reproduction (Oxford, England)|October 18, 2017
Chromosomal abnormalities in 1663 infertile men with azoospermia: the clinical consequencesR B Donker, V Vloeberghs, H Groen, et al.Genes, Brain, and Behavior|January 30, 2016
Neuropsychological phenotype and psychopathology in seven adult patients with Phelan-McDermid syndrome: implications for treatment strategyJ I M Egger, R J Zwanenburg, C M A van Ravenswaaij-Arts, et al.Human Reproduction (Oxford, England)|June 29, 2012
Chromosomal abnormalities in azoospermic and non-azoospermic infertile men: numbers needed to be screened to prevent adverse pregnancy outcomesE C Dul, J van Echten-Arends, H Groen, et al.American Journal of Medical Genetics. Part A|April 25, 2015
3p14 deletion is a rare contiguous gene syndrome: report of 2 new patients and an overview of 14 patientsB I Dimitrov, C Ogilvie, D Wieczorek, et al.Human Reproduction (Oxford, England)|November 15, 2011
The prevalence of chromosomal abnormalities in subgroups of infertile menE C Dul, H Groen, C M A van Ravenswaaij-Arts, et al.Pageof 4