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European Journal of Pediatrics|May 14, 1998
Vesico-ureteral reflux: a genetic condition?K Devriendt, P Groenen, H Van Esch, et al.
American Journal of Medical Genetics|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, K Devriendt, A Swillen, et al.
Human Genetics|October 6, 1998
Missense mutation and hexanucleotide duplication in the PAX2 gene in two unrelated families with renal-coloboma syndrome (MIM 120330)K Devriendt, G Matthijs, B Van Damme, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Psychotic disorders in Prader-Willi syndromeA Vogels, M De Hert, M J Descheemaeker, et al.
Annals of Neurology|October 23, 1997
The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigreesS Claes, K Devriendt, L Lagae, et al.
Prenatal Diagnosis|December 18, 2001
Semilobar holoprosencephaly in a 46,XY female fetusI Witters, P Moerman, M Muenke, et al.
European Journal of Medical Genetics|December 28, 2005
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD)Ph Debeer, H Van Esch, C Huysmans, et al.
Annals of Neurology|November 1, 1996
Clinical and molecular genetic features of congenital spinal muscular atrophyK Devriendt, M Lammens, E Schollen, et al.
Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, et al.
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