The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disability-Reference-Cited by-同舟云学术

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The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disability

Published:2023-01 Issue: Volume:538 Page:94-103
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Zhang Hongyun,Chen Xin,Tan Hu,Teng Yanling,Liu Dihua,Wu Jiayu,Duan Ranhui,Liang Desheng,Li Zhuo,Wu Lingqian

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference45 articles.

1. Intellectual developmental disorders”: reflections on the international consensus document for redefining “mental retardation-intellectual disability” in ICD-11;Bertelli;Adv Ment Health Intellect Disabil,2016

2. Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families;Harripaul;Mol. Psychiatry.,2018

3. Genomic diagnosis for children with intellectual disability and/or developmental delay;Bowling;Genome Med.,2017

4. Comorbidities associated with genetic abnormalities in children with intellectual disability;Chen;Sci. Rep.,2021

5. Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing;Redin;J. Med. Genet.,2014

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Testing for Global Developmental Delay in Early Childhood;JAMA Network Open;2024-06-05

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