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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Détails bibliographiques
Publié dans:Noro Psikiyatr Ars
Auteurs principaux: 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
Langue:Inglês
Publié: Noro-Psikiyatri Arsivi 2020
Sujets:
Research Article
Accès en ligne: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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