Whole-Exome Sequencing for Identifying Genetic Causes of Intellectual Developmental Disorders
Author:
Publisher
Informa UK Limited
Subject
General Medicine
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1. Vesicular CLC chloride/proton exchangers in health and diseases;Frontiers in Pharmacology;2023-11-07
2. Novel variants in the CLCN4 gene associated with syndromic X-linked intellectual disability;Frontiers in Neurology;2023-09-15
3. Meta-analysis of the diagnostic and clinical utility of exome and genome sequencing in pediatric and adult patients with rare diseases across diverse populations;Genetics in Medicine;2023-09
4. Diverse Clinical Phenotypes of CASK-Related Disorders and Multiple Functional Domains of CASK Protein;Genes;2023-08-20
5. Genome-Wide Sequencing Modalities for Children with Unexplained Global Developmental Delay and Intellectual Disabilities—A Narrative Review;Children;2023-03-03
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