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Annales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.Clinical Genetics|December 17, 2009
DISC1 duplication in two brothers with autism and mild mental retardationA Crepel, J Breckpot, J-P Fryns, et al.European Journal of Pediatrics|October 1, 1994
Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblingsK Devriendt, A Casaer, A Van Cauter, et al.Journal of Medical Genetics|June 30, 2000
Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?H C Janssen, C Schaap, N Vandevijver, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|December 23, 2004
Ibuprofen and cerebral oxygenation and circulationG Naulaers, G Delanghe, K Allegaert, et al.Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.American Journal of Medical Genetics|February 22, 2002
Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler typeI Witters, Ph Moerman, K Devriendt, et al.European Journal of Medical Genetics|June 5, 2012
Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variantsM Isrie, G Froyen, K Devriendt, et al.Neuropediatrics|April 1, 1997
Fetal akinesia sequence caused by nemaline myopathyM Lammens, P Moerman, J P Fryns, et al.European Journal of Pediatrics|May 14, 1998
Vesico-ureteral reflux: a genetic condition?K Devriendt, P Groenen, H Van Esch, et al.Pageof 105