Chargement en cours...

Phenotypic Variations in Wolf-Hirschhorn Syndrome

Wolf-Hirschhorn syndrome (WHS) is a rare chromosomal disorder caused by terminal deletion of the short arm of chromosome 4. The clinical picture includes growth retardation, severe mental retardation, characteristic “Greek helmet” like face, seizures and midline defects in the brain, heart, palate a...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Balkan J Med Genet
Auteurs principaux: Sukarova-Angelovska, E, Kocova, M, Sabolich, V, Palcevska, S, Angelkova, N
Format: Artigo
Langue:Inglês
Publié: Macedonian Science of Sciences and Arts 2014
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4347473/
https://ncbi.nlm.nih.gov/pubmed/25741211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/bjmg-2014-0021
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!