The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS)()

With advances in laboratory technology, an increasing number of potentially pathogenic CNVs is recognised. The phenotypic effects of some CNVs are well characterised, however, it remains unclear how much information reaches the parents of affected children and by what route. The 22q11.2 deletion syn...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: van den Bree, Marianne B.M., Miller, Gregory, Mansell, Elizabeth, Thapar, Anita, Flinter, Frances, Owen, Michael J.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2013
Schlagworte:
Genetic Forum
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3744815/
https://ncbi.nlm.nih.gov/pubmed/23707654
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejmg.2013.05.001
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge