Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability

Chromosomal microarray (CMA) analysis for discovery of copy number variants (CNVs) is now recommended as a first-line diagnostic tool in patients with unexplained developmental delay/intellectual disability (DD/ID) and autism spectrum disorders. In this study, we present the results of CMA analysis...

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Detaylı Bibliyografya
Yayımlandı:J Pediatr Genet
Asıl Yazarlar: Arican, Pinar, Olgac Dundar, Nihal, Ozyilmaz, Berk, Cavusoglu, Dilek, Gencpinar, Pinar, Erdogan, Kadri Murat, Saka Guvenc, Merve
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Georg Thieme Verlag KG 2019
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6375720/
https://ncbi.nlm.nih.gov/pubmed/30775046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0038-1676583
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