Early developmental concerns in 22q11.2 deletion and duplication carriers

Author:

Kortanek Eve S.,McDonald Nicole M.,Nosco Erin E.,MacNaughton Gabrielle A.,Lin Amy,Jeste Shafali S.,Bearden Carrie E.

Publisher

Elsevier BV

Subject

Psychiatry and Mental health,Clinical Psychology,Developmental and Educational Psychology

Reference49 articles.

1. Using a parent survey to advance knowledge about the nature and consequences of fragile X syndrome;Bailey;American Journal on Intellectual and Developmental Disabilities,2010

2. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;The Journal of Pediatrics,2011

3. Ages & stages questionnaires: A parent-completed, child-monitoring system;Bricker,1999

4. Clinical features and follow-up in patients with 22q11.2 deletion syndrome;Cancrini;The Journal of Pediatrics,2014

5. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants;Chawner;American Journal of Psychiatry,2021

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