Clinical and molecular characterization of patients with distal 11q deletions. - Abstract - Europe PMC
PDF) Fryns syndrome without diaphragmatic hernia, DOOR syndrome or Fryns-like syndrome? Report on patients from Indian Ocean islands | Fabrice Cuillier, Jean-luc Alessandri, and Sylvain Samperiz - Academia.edu
Journal of Communication Disorders 2004: Vol 37 Table of Contents : Free Download, Borrow, and Streaming : Internet Archive
Improved Molecular Diagnostics of Idiopathic Short Stature and Allied Disorders: Quantitative Polymerase Chain Reaction-Based Co
Association of distal arthrogryposis, mental retardation, whistling face, and pierre robin sequence: Evidence for nosologic hete
Longitudinal Phenotypic Analysis in Patients with Connexin 26 (GJB2) (DFNB1) and Connexin 30 (GJB6) Mutations
Jean-Pierre Fryns: H-index & Awards - Academic Profile | Research.com
Family Contexts, Parental Behaviour, and Personality Profiles of Children and Adolescents with Prader-Willi, Fragile-X, or Will
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome. - Abstract - Europe PMC
File:Lujan.jpg - Wikimedia Commons
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
Opitz C syndrome and pseudohypoaldosteronism
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
Amazon.in: Van Gerry - Biology & Life Sciences / Sciences, Technology & Medicine: Books
Jean-Pierre Améris - Wikipedia
Jean-Pierre Fryns: H-index & Awards - Academic Profile | Research.com
Jean-Pierre FRYNS | KU Leuven, Leuven | ku leuven | Department of Human Genetics - Page 2
Report A Mutation in the Rett Syndrome Gene, MECP2, Causes X-Linked Mental Retardation and Progressive Spasticity in Males
Jean-Pierre FRYNS | KU Leuven, Leuven | ku leuven | Department of Human Genetics - Page 2
Increased frequency of chromosomal abnormalities in female partners of couples undergoing in vitro fertilization or intracytopla
The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly
Fonds eert geneticus Herman Van den Berghe - Nieuws
BIOGRAFÍAS MÉDICAS ILUSTRADAS: DR. JEAN-PIERRE FRYNS
