Clinical use of whole exome sequencing in children with developmental delay/intellectual disability-Reference-Cited by-同舟云学术

Clinical use of whole exome sequencing in children with developmental delay/intellectual disability

Published:2024-09 Issue:5 Volume:65 Page:445-450
ISSN:1875-9572
Container-title:Pediatrics & Neonatology
language:en
Short-container-title:Pediatrics & Neonatology

Author:

Jo Yoon Hee^ORCID,Choi Soo Han,Yoo Hye Won,Kwak Min Jung,Park Kyung Hee,Kong Juhyun,Lee Yun-Jin,Nam Sang Ook,Lee Bo Lyun,Chung Woo Yeong,Oh Seung Hwan,Kim Young Mi^ORCID

Publisher

Elsevier BV

Reference21 articles.

1. Genetic analysis of children with unexplained developmental delay and/or intellectual disability by whole-exome sequencing;Xiang;Front Genet,2021

2. Targeted next-generation sequencing of Korean patients with developmental delay and/or intellectual disability;Han;Front Pediatr,2018

3. Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG);Manickam;Genet Med,2021

4. Utility of chromosomal microarray in children with unexplained developmental delay/intellectual disability;Kamath;Fetal Pediatr Pathol,2022

5. Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability;Han;Clin Exp Pediatr,2020

Cited by 3 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. Comprehensive evaluation of the child with global developmental delays or intellectual disability;Clinical and Experimental Pediatrics;2024-09-15

2. Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability—An Exception or a Necessity?;Genes;2024-06-15

3. Rare Genetic Developmental Disabilities: Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) Disorders;Genes;2024-05-14