Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability-Reference-Cited by-同舟云学术

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Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability

Published:2020-07-23 Issue: Volume: Page:1-11
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Kamath Vandana¹^ORCID,Yoganathan Sangeetha²,Thomas Maya Mary²,Gowri Mahasampath³,Chacko Mary Purna¹

Affiliation:

1. Department of Cytogenetics, Christian Medical College and Hospital, Vellore, India

2. Department of Neurological Sciences, Christian Medical College and Hospital, Vellore, India

3. Department of Biostatistics, Christian Medical College and Hospital, Vellore, India

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2020.1791292

Reference28 articles.

1. Clinical Genetic Evaluation of the Child With Mental Retardation or Developmental Delays

2. Practice parameter: Evaluation of the child with global developmental delay [RETIRED]

3. Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions

Cited by 6 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. Clinical use of whole exome sequencing in children with developmental delay/intellectual disability;Pediatrics & Neonatology;2024-09

3. Combining chromosomal microarray and clinical exome sequencing for genetic diagnosis of intellectual disability;Scientific Reports;2023-12-20

4. Genome-Wide Sequencing Modalities for Children with Unexplained Global Developmental Delay and Intellectual Disabilities—A Narrative Review;Children;2023-03-03

5. Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy;Molecular Syndromology;2023

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