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American Journal of Medical Genetics. Part A|December 12, 2002
A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasksJean Steyaert, Eric Legius, Martine Borghgraef, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
Toriello-Carey syndrome with a 6Mb interstitial deletion at 22q12 detected by array CGHEdith Said, Alfred Cuschieri, Joris Vermeesch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2009
Diagnosis of miscarriages by molecular karyotyping: benefits and pitfallsCaroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, et al.
European Journal of Medical Genetics|February 24, 2009
Congenital diaphragmatic hernia is part of the new 15q24 microdeletion syndromeHilde Van Esch, Liesbeth Backx, Elly Pijkels, et al.
European Journal of Medical Genetics|August 2, 2005
Follow-up of adult males with chromosome 18p deletionThomy J L de Ravel, Paul Thiry, Jean-Pierre Fryns
American Journal of Medical Genetics. Part A|April 29, 2006
Pervasive developmental disorders in Prader-Willi syndrome: the Leuven experience in 59 subjects and controlsMie-Jef Descheemaeker, Veerle Govers, Peter Vermeulen, et al.
Fertility and Sterility|February 28, 2006
High frequency of iatrogenic monozygotic twins with administration of clomiphene citrate and a change in chorionicityCatherine Derom, Fernand Leroy, Robert Vlietinck, et al.
Clinical Dysmorphology|September 15, 2004
A boy with an unusual association of ventral midline anomalies including a trunk-like umbilicusHilde Van Esch, Paul Mariën, Maryse De Smedt, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutation in a large family with Noonan syndrome and dizygous twinningEls Schollen, Gert Matthijs, Marc Gewillig, et al.
Human Molecular Genetics|August 13, 2003
Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasiaAnil K Agarwal, Jean-Pierre Fryns, Richard J Auchus, et al.
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