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American Journal of Perinatology|April 26, 2001
Aneurysm of the ductus arteriosus in a neonate with 13q-deletionG Naulaers, K Devriendt, P Moerman, et al.American Journal of Medical Genetics|May 22, 1995
Diaphragmatic hernia in Denys-Drash syndromeK Devriendt, E Deloof, P Moerman, et al.Prenatal Diagnosis|May 1, 1996
Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndromeK Devriendt, K van den Berghe, P Moerman, et al.Clinical Genetics|April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletionK Devriendt, R Van Hoestenberghe, C Van Hole, et al.Journal of Medical Genetics|February 25, 1998
Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entityK Devriendt, L Standaert, C Van Hole, et al.American Journal of Medical Genetics|May 1, 1987
Congenital eventration of the diaphragm: an unusual cause of intractable neonatal respiratory distress with variable etiologyP Moerman, J P Fryns, H Devlieger, et al.American Journal of Medical Genetics|December 1, 1988
The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndromeP Moerman, J P Fryns, K Vandenberghe, et al.Histopathology|October 1, 1992
Pathogenesis of congenital cystic adenomatoid malformation of the lungP Moerman, J P Fryns, K Vandenberghe, et al.Journal of Medical Genetics|May 1, 1997
Chromosome 22q11 deletion presenting as the Potter sequenceK Devriendt, P Moerman, D Van Schoubroeck, et al.Prenatal Diagnosis|May 23, 2000
Diaphragmatic hernia as the first echographic sign in Apert syndromeI Witters, K Devriendt, P Moerman, et al.Pageof 105