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...

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Detalles Bibliográficos
Autores principales: van den Bree, Marianne B.M., Miller, Gregory, Mansell, Elizabeth, Thapar, Anita, Flinter, Frances, Owen, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Genetic Forum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744815/
https://www.ncbi.nlm.nih.gov/pubmed/23707654
http://dx.doi.org/10.1016/j.ejmg.2013.05.001

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