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Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Craniofrontonasal dysplasia: more severe expression in the mother than in her sonK Devriendt, C Van Mol, J P FrynsPediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|July 1, 1997
Lymphangiomatosis of the body wall: a report of two cases associated with chylothorax and fatal outcomeP Moerman, C Van Geet, H DevliegerPrenatal Diagnosis|December 18, 2001
Semilobar holoprosencephaly in a 46,XY female fetusI Witters, P Moerman, M Muenke, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocationS G Frints, P Moerman, J P FrynsAnnals of Neurology|November 1, 1996
Clinical and molecular genetic features of congenital spinal muscular atrophyK Devriendt, M Lammens, E Schollen, et al.American Journal of Perinatology|August 24, 1999
Management of severe neonatal anemia due to fetomaternal transfusionG Naulaers, S Barten, C Vanhole, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|July 1, 1997
Use of methohexital for elective intubation in neonatesG Naulaers, E Deloof, C Vanhole, et al.Annales De Genetique|August 26, 1998
Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the motherJ P Fryns, E Smeets, K Devriendt, et al.Clinical Dysmorphology|May 18, 1999
Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocationT Lukusa, K Devriendt, J Jaeken, et al.American Journal of Medical Genetics|February 17, 2001
Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsA Swillen, A Vogels, K Devriendt, et al.Pageof 105