Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome

BACKGROUND: 3q29 deletion syndrome is caused by a recurrent hemizygous 1.6 Mb deletion on the long arm of chromosome 3. The syndrome is rare (1 in 30,000 individuals) and is associated with mild to moderate intellectual disability, increased risk for autism and anxiety, and a 40-fold increased risk...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:BMC Psychiatry
Autors principals: Murphy, Melissa M., Lindsey Burrell, T., Cubells, Joseph F., España, Roberto Antonio, Gambello, Michael J., Goines, Katrina C. B., Klaiman, Cheryl, Li, Longchuan, Novacek, Derek M., Papetti, Ava, Sanchez Russo, Rossana Lucia, Saulnier, Celine A., Shultz, Sarah, Walker, Elaine, Mulle, Jennifer Gladys
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2018
Matèries:
Study Protocol
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5994080/
https://ncbi.nlm.nih.gov/pubmed/29884173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12888-018-1760-5
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars