Yield of array‐ <scp>CGH</scp> analysis in Tunisian children with autism spectrum disorder-Reference-Cited by-同舟云学术

Yield of array‐ CGH analysis in Tunisian children with autism spectrum disorder

Published:2022-06-27 Issue:8 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Chehbani Fethia¹²^ORCID,Tomaiuolo Pasquale³^ORCID,Picinelli Chiara³,Baccarin Marco³⁴,Castronovo Paola³,Scattoni Maria Luisa⁵^ORCID,Gaddour Naoufel⁶,Persico Antonio M.⁷^ORCID

Affiliation:

1. Department of Psychiatry, Research Laboratory “Vulnerability to Psychotic Disorders LR 05 ES 10” Monastir University Hospital Monastir Tunisia

2. Faculty of Pharmacy University of Monastir Monastir Tunisia

3. Mafalda Luce Center for Pervasive Developmental Disorders Milan Italy

4. Department of Genetics Synlab Suisse SA Bioggio Switzerland

5. Research Coordination and Support Service Istituto Superiore di Sanità Rome Italy

6. Unit of Child Psychiatry Monastir University Hospital Monastir Tunisia

7. Child & Adolescent Neuropsychiatry Program Modena University Hospital & Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia Modena Italy

Funder

Université Monastir

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1939

Reference84 articles.

1. Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion

2. Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features

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