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American Journal of Medical Genetics|October 26, 2002
Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnosesIngrid Witters, Philippe Moerman, Jean-Pierre FrynsPrenatal Diagnosis|August 10, 2004
Positive maternal serum triple test screening in severe early onset hypophosphatasiaIngrid Witters, Philippe Moerman, Etienne Mornet, et al.Fetal Diagnosis and Therapy|December 16, 2005
Fetal magnetic resonance imaging of an intracranial venous thrombosis. Case reportLuc Breysem, Ingrid Witters, Bernard Spitz, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 12, 2002
Benign multiple diffuse neonatal hemangiomatosis after a pregnancy complicated by polyhydramnios and a placental chorioangiomaIngrid Witters, Marie Therèse Van Damme, Paul Ramaekers, et al.Prenatal Diagnosis|January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)Ingrid Witters, K Devriendt, E Legius, et al.European Child & Adolescent Psychiatry|December 7, 2002
Psychiatric genetics: the case of single gene disordersJean Steyaert, Jean-Pierre FrynsPrenatal Diagnosis|December 23, 2004
Post-zygotic origin of isochromosome 12pThomy J L de Ravel, Kathelijn Keymolen, Elvire van Assche, et al.European Journal of Human Genetics : EJHG|May 21, 2009
Angelman syndrome (AS, MIM 105830)Griet Van Buggenhout, Jean-Pierre FrynsOrphanet Journal of Rare Diseases|July 13, 2006
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)Griet Van Buggenhout, Jean-Pierre FrynsPageof 25