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Paediatric and Perinatal Epidemiology|January 27, 2005
Gender mix: does it modify birthweight--outcome association?Robert Derom, Catherine Derom, Ruth J F Loos, et al.
European Journal of Medical Genetics|July 5, 2008
The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvementIsabelle Bailleul-Forestier, Ariane Berdal, Frans Vinckier, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Psychological distress in the 5-year period after predictive testing for Huntington's diseaseMarleen Decruyenaere, Gerry Evers-Kiebooms, Trees Cloostermans, et al.
European Journal of Medical Genetics|August 2, 2005
X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian familyHilde Van Esch, Ginevra Zanni, Maureen Holvoet, et al.
Obesity (Silver Spring, Md.)|January 29, 2011
DNA methylation variability at growth-related imprints does not contribute to overweight in monozygotic twins discordant for BMINicole Y P Souren, Sascha Tierling, Jean-Pierre Fryns, et al.
Fetal Diagnosis and Therapy|December 15, 2010
Recent developments in the genetic factors underlying congenital diaphragmatic herniaPaul D Brady, Kasemsri Srisupundit, Koenraad Devriendt, et al.
European Journal of Human Genetics : EJHG|August 13, 2002
Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD)Geneviève Michils, Sabine Tejpar, Jean-Pierre Fryns, et al.
Molecular Cytogenetics|April 12, 2012
Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicismCaroline Robberecht, Thierry Voet, Gülen E Utine, et al.
Developmental Medicine and Child Neurology|November 18, 2005
Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defectAnn Swillen, Hilde Feys, Tamara Adriaens, et al.
The Journal of Urology|August 30, 2008
Testicular histology in boys with Prader-Willi syndrome: fertile or infertile?Annick Vogels, Philippe Moerman, Jean-Pierre Frijns, et al.
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