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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Bibliografische gegevens
Gepubliceerd in:Noro Psikiyatr Ars
Hoofdauteurs: Gürkan, Hakan, Atli, Emine İkbal, Atli, Engin, Bozatli, Leyla, Altay, Mengühan Araz, Yalçintepe, Sinem, Özen, Yasemin, Eker, Damla, Akurut, Çisem, Demır, Selma, Görker, Işık
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Noro-Psikiyatri Arsivi 2020
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Research Article
Online toegang: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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