Chromosomal Microarray Testing in 42 Korean Patients with Unexplained Developmental Delay, Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies

Chromosomal microarray (CMA) is a high-resolution, high-throughput method of identifying submicroscopic genomic copy number variations (CNVs). CMA has been established as the first-line diagnostic test for individuals with developmental delay (DD), intellectual disability (ID), autism spectrum disor...

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Detalles Bibliográficos
Autores principales: Lee, Sun Ho, Song, Wung Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637341/
https://www.ncbi.nlm.nih.gov/pubmed/29020723
http://dx.doi.org/10.5808/GI.2017.15.3.82

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637341/
https://www.ncbi.nlm.nih.gov/pubmed/29020723
http://dx.doi.org/10.5808/GI.2017.15.3.82

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