Open AccessMultiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder
Author(s) -
Safiah Alhazmi,
Maryam Alzahrani,
Reem M. Farsi,
Mona G. Alharbi,
Khloud Algothmi,
Najla Ali Alburae,
Magdah Ganash,
Sheren A. Azhari,
Fatemah Basingab,
Asma Almuhammadi,
Amany I. Alqosaibi,
Heba Alkhatabi,
Aisha Elaimi,
Mohammed M. Jan,
Hesham Aldhalaan,
Aziza Alrafiah,
Aisha Alrofaidi
Publication year - 2022
Publication title -
pharmacogenomics and personalized medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.845
H-Index - 28
ISSN - 1178-7066
DOI - 10.2147/pgpm.s366826
Subject(s) - medicine , copy number variation , autism spectrum disorder , deletion syndrome , chromosome , autism , genetics , genome , psychiatry , gene , biology , phenotype