Jean‐Pierre Frijns

Preimplantation genetic screening for aneuploidy of embryos after in vitro fertilization in women aged at least 35 years: a prospective randomized trial

Sophie Debrock, Cindy Melotte, Carl Spiessens et al. · Fertility and Sterility · 2009 · 146 citations · Full text

Infertility, Developmental Biology, Fertility +15

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills

A Denayer, Hilde Van Esch, Thomy de Ravel et al. · Molecular Syndromology · 2012 · 99 citations · Full text

The Wiedemann-Rautenstrauch or neonatal progeroid syndrome

E. Devos, Jules G. Leroy, Jean‐Pierre Frijns et al. · European Journal of Pediatrics · 1981 · 53 citations

Neonatal Progeroid Syndrome, Neonatology, Pathogenesis +6

3‐Phosphoglycerate dehydrogenase deficiency and 3‐phosphoserine phosphatase deficiency: Inborn errors of serine biosynthesis

J. Jaeken, Michel Detheux, Lionel Van Maldergem et al. · Journal of Inherited Metabolic Disease · 1996 · 50 citations

Mutation analysis in Costello syndrome: functional and structural characterization of the<i>HRAS</i>p.Lys117Arg mutation

Ellen Denayer, Annabel Parret, Magdalena Chmara et al. · Human Mutation · 2007 · 50 citations

Mental Retardation Syndrome, Structural Characterization, Signal Transduction +13