Copy number variation analysis of patients with intellectual disability from North-West Spain

Author:

Quintela Inés,Eirís Jesús,Gómez-Lado Carmen,Pérez-Gay Laura,Dacruz David,Cruz Raquel,Castro-Gago Manuel,Míguez Luz,Carracedo Ángel,Barros Francisco

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference101 articles.

1. 1.39Mb inherited interstitial deletion in 12p13.33 associated with developmental delay;Abdelmoity;Eur J Med Genet,2011

2. Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8700 patients;Ahn;Mol. Cytogenet.,2013

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

4. Diagnostic and Statistical Manual of Mental Disorders;APA,2013

5. Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability;Bartnik;J. Appl. Genet.,2013

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