The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disability
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference45 articles.
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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
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