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Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescenceA Swillen, K Devriendt, E Legius, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|August 5, 2000
Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?A Swillen, L Vandeputte, J Cracco, et al.
Prenatal Diagnosis|October 15, 2013
Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic herniaP D Brady, P DeKoninck, J P Fryns, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.
Genetic Counseling (Geneva, Switzerland)|June 21, 2008
Cognitive correlates of mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.
Human Genetics|November 1, 1989
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosomeJ Zhang, P Marynen, K Devriendt, et al.
American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
American Journal of Medical Genetics|January 11, 1996
Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalitiesK Devriendt, J van den Oord, R De Vos, et al.
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