Prenatal Diagnosis of Hemimegalencephaly: Report of Two Cases - Ingrid Witters, Mieke Cannie, Jean-Pierre Fryns, Marcel De Bruyne, Françoise Laverge, Philippe Delattin, Piet Claerhout, Philippe Moerman, 2006
A microdeletion proximal of the critical deletion region is associated with mild WolfHirschhorn syndrome
Structural chromosome rearrangements in couples with recurrent fetal wastage
PDF) Fryns syndrome: A variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia
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Jean-Pierre FRYNS | KU Leuven, Leuven | ku leuven | Department of Human Genetics | Research profile
Short limbed dwarfism, genital hypoplasia, sparse hair, and vertebral anomalies: a variant of Ellis-van Creveld syndrome?
Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia Alexandre Irrthum, - ppt download
Jean-Pierre FRYNS | KU Leuven, Leuven | ku leuven | Department of Human Genetics | Research profile - Page 2
Historie | Klinische Genetica
Fryns, JP
Mild phenotype and normal gonadal function in females with 4p trisomy due to unbalanced t(X;4)(p22.1;p14)
marcel fryns - AbeBooks
L'élève du compléxe scolaire MGR JEAN FRYNS
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus) | springermedizin.de
Jean-Pierre FRYNS | KU Leuven, Leuven | ku leuven | Department of Human Genetics | Research profile - Page 2
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
Lujan–Fryns syndrome - Wikiwand
retinopathy: confirmation of a new type of arthrogryposis
Fryns, JP
Fryns, JP
Jean-Pierre Fryns: H-index & Awards - Academic Profile | Research.com
Jean-Pierre Fryns: H-index & Awards - Academic Profile | Research.com
Isabelle MARCEAU FRYNS | Résidences Funéraires Goyer
100+ profils pour “Fryns” | LinkedIn
Pierre Fryns - Freelance | LinkedIn
duplication Mecp2 français
Pericardial effusion in the first trimester of pregnancy - Witters - 2011 - Prenatal Diagnosis - Wiley Online Library
