Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems-Reference-Cited by-同舟云学术

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

Published:2020 Issue:2 Volume:11 Page:62-72
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Farajzadeh Valilou Saeed,Alavi Afagh,Pashaei Mahdiyeh,Ghasemi Firouzabadi Saghar,Shafeghati Yousef,Nozari Ahoura,Hadipour Fatemeh,Hadipour Zahra,Maghsoodlou Estrabadi Bijan,Gholamreza Noorazar Seyed,Banihashemi Susan,Karimian Javad,Fattahi Mahshid,Behjati Farkhondeh

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

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4. Baio J, Wiggins L, Christensen DL, Maenner MJ, Daniels J, et al: Prevalence of autism spectrum disorder among children aged 8 years. MMWR Surveill Summ 67:1-23 (2018).

5. Balasubramanian M, Jones R, Milne E, Marshall C, Arundel P, et al: Autism and heritable bone fragility: a true association? Bone Rep 8:156-162 (2018).

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