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Molecular Syndromology 2020 / 3

Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems

Farajzadeh Valilou, Saeed, Alavi, Afagh, Pashaei, Mahdiyeh, Ghasemi Firouzabadi, Saghar, Shafeghati, Yousef, Nozari, Ahoura, Hadipour, Fatemeh, Hadipour, Zahra, Maghsoodlou Estrabadi, Bijan, Gholamrez
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Language:
english
Journal:
Molecular Syndromology
DOI:
10.1159/000506530
Date:
March, 2020
File:
PDF, 1.02 MB
english, 2020
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