Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders

INTRODUCTION: Aneuploids, copy number variations (CNVs), and single nucleotide variants in specific genes are the main genetic causes of developmental delay (DD) and intellectual disability disorder (IDD). These genetic changes can be detected using chromosome analysis, chromosomal microarray (CMA),...

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Bibliografski detalji
Izdano u:Noro Psikiyatr Ars
Glavni autori: Gürkan, Hakan, Atli, Emine İkbal, Atli, Engin, Bozatli, Leyla, Altay, Mengühan Araz, Yalçintepe, Sinem, Özen, Yasemin, Eker, Damla, Akurut, Çisem, Demır, Selma, Görker, Işık
Format: Artigo
Jezik:Inglês
Izdano: Noro-Psikiyatri Arsivi 2020
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7481981/
https://ncbi.nlm.nih.gov/pubmed/32952419
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.29399/npa.24890
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