FMR1 premutation in children with autism spectrum disorders: Should additional diagnostic tests be performed?
Author:
Affiliation:
1. Centro de Estudos do Genoma Humano e Células‐tronco, Departamento de Genética e Biologia Evolutiva, Instituto de Biociências Universidade de São Paulo São Paulo Brazil
2. Instituto de Psicologia Universidade de São Paulo São Paulo Brazil
Funder
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Fundação de Amparo à Pesquisa do Estado de São Paulo
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62624
Reference32 articles.
1. A genome-wide scan for common alleles affecting risk for autism
2. Clinical features of boys with fragile X premutations and intermediate alleles
3. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray
4. Co-occurring conditions associated withFMR1gene variations: Findings from a national parent survey
5. Wolf-Hirschhorn syndrome: A review and update
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