Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion-Reference-Cited by-同舟云学术

Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion

Published:2015-08-29 Issue:12 Volume:167 Page:3121-3129
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Quintela Ines¹,Gomez-Guerrero Lorena²,Fernandez-Prieto Montse²,Resches Mariela³,Barros Francisco²,Carracedo Angel¹²⁴

Affiliation:

1. Grupo de Medicina Xenomica; Universidade de Santiago de Compostela; Centro Nacional de Genotipado-Plataforma de Recursos Biomoleculares y Bioinformaticos-Instituto de Salud Carlos III (CeGen-PRB2-ISCIII); Santiago de Compostela Spain

2. Grupo de Medicina Xenomica; CIBERER; Fundacion Publica Galega de Medicina Xenomica-SERGAS; Santiago de Compostela Spain

3. Departamento de Psicologia Evolutiva y de la Educacion; Universidade de Santiago de Compostela; Santiago de Compostela Spain

4. Center of Excellence in Genomic Medicine Research; King Abdulaziz University; Jeddah Saudi Arabia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37292/fullpdf

Reference37 articles.

1. A high-density SNP genome-wide linkage scan in a large autism extended pedigree;Allen-Brady;Mol Psychiatry,2009

2. Ccdc80-l1 is involved in axon pathfinding of zebrafish motoneurons;Brusegan;PLoS ONE,2012