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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:BMC Psychiatry
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BioMed Central 2018
विषय:
Study Protocol
ऑनलाइन पहुंच: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
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