Fonds eert geneticus Herman Van den Berghe - Nieuws
Family Contexts, Parental Behaviour, and Personality Profiles of Children and Adolescents with Prader-Willi, Fragile-X, or Will
Jean-Pierre Fryns: H-index & Awards - Academic Profile | Research.com
Historie | Klinische Genetica
Prader-Willi syndrome in a child with mosaic analysis
The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly
NAGER TYPE OF ACROFACIAL DYSOSTOSIS: AN EXAMPLE OF AUTOSOMAL DOMINANT TRANSMISSION WITH VARIABLE EXPRESSION 1 The syndrome combi
File:Lujan.jpg - Wikimedia Commons
Increased frequency of chromosomal abnormalities in female partners of couples undergoing in vitro fertilization or intracytopla
Jean-Pierre FRYNS | KU Leuven, Leuven | ku leuven | Department of Human Genetics - Page 2
retinopathy: confirmation of a new type of arthrogryposis
Tentative clinical diagnosis of Lujan-Fryns syndrome—A conglomeration of different genetic entities?
Report Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size
Journal of Communication Disorders 2004: Vol 37 Table of Contents : Free Download, Borrow, and Streaming : Internet Archive
PDF) PTEN mutation in a family with Cowden syndrome and autism | Ann Swillen - Academia.edu
Longitudinal Phenotypic Analysis in Patients with Connexin 26 (GJB2) (DFNB1) and Connexin 30 (GJB6) Mutations
Jean-Pierre Améris - Wikipedia
Report A Mutation in the Rett Syndrome Gene, MECP2, Causes X-Linked Mental Retardation and Progressive Spasticity in Males
Jean-Pierre Fryns: H-index & Awards - Academic Profile | Research.com
Pfeiffer syndrome
Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular. - ppt download
X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11
Clinical and molecular characterization of patients with distal 11q deletions. - Abstract - Europe PMC
Improved Molecular Diagnostics of Idiopathic Short Stature and Allied Disorders: Quantitative Polymerase Chain Reaction-Based Co
Fryns, JP
