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AB024. Chromosome microarray analysis (CMA) for the diagnosis of children with developmental delay and multiple congenital anomalies in Singapore

Chromosome microarray analysis (CMA) is a sensitive method to identify submicroscopic changes too small to be detected by conventional karyotyping. Due to its high-sensitivity in identifying regions with structural variation and hence the genes involved, it is recommended to be the first-tier geneti...

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Publicat a:Ann Transl Med
Autors principals: Law, Hai-Yang, Brett, Maggie, Tan, Ene-Choo, Yong, Min-Hwee, Lai, Angeline
Format: Artigo
Idioma:Inglês
Publicat: AME Publishing Company 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563548/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB024
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