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American Journal of Medical Genetics|October 12, 2002
Clinical study and haplotype analysis in two brothers with Partington syndromeSuzanna G M Frints, Martine Borghgraef, Guy Froyen, et al.
Nature Reviews. Genetics|August 19, 2011
Advances in prenatal screening: the ethical dimensionAntina de Jong, Wybo J Dondorp, Suzanna G M Frints, et al.
Human Reproduction (Oxford, England)|August 16, 2011
Non-invasive prenatal diagnosis for aneuploidy: toward an integral ethical assessmentAntina de Jong, Wybo J Dondorp, Suzanna G M Frints, et al.
Human Mutation|June 5, 2007
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genesGuy Froyen, Hilde Van Esch, Marijke Bauters, et al.
Clinical Chemistry|October 16, 2015
Cell-Free RNA Is a Reliable Fetoplacental Marker in Noninvasive Fetal Sex DeterminationElke Mersy, Brigitte H W Faas, Sabine Spierts, et al.
Public Health Genomics|July 24, 2015
Advantages and Disadvantages of Different Implementation Strategies of Non-Invasive Prenatal Testing in Down Syndrome Screening ProgrammesElke Mersy, Christine E M de Die-Smulders, Audrey B C Coumans, et al.
Human Mutation|October 23, 2009
Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exonLuciana Musante, Stella-Amrei Kunde, Tina O Sulistio, et al.
Human Molecular Genetics|June 19, 2003
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behaviorSuzanna G M Frints, Peter Marynen, Dieter Hartmann, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|September 11, 2012
LPS-induced chorioamnionitis and antenatal corticosteroids modulate Shh signaling in the ovine fetal lungJennifer J P Collins, Elke Kuypers, Ilias Nitsos, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 geneSuzanna G M Frints, Lin Jun, Jean-Pierre Fryns, et al.
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