Chargement en cours...

Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes

BACKGROUND: Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are clinically distinct neurodevelopmental genetic disorders that map to 15q11-q13. The primary phenotypes are attributable to loss of expression of imprinted genes within this region which can arise by means of a number of mechanism...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Ramsden, Simon C, Clayton-Smith, Jill, Birch, Rachael, Buiting, Karin
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2010
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2877670/
https://ncbi.nlm.nih.gov/pubmed/20459762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-70
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!