Copy number variations on chromosome 15 detected by molecular karyotyping in patients with developmental delay and congenital anomalies

Introduction: Global developmental delay (GDD) and congenital anomalies represent a heterogeneous group of medical conditions that may have a known genetic etiology. Molecular karyotyping is the gold standard for detecting copy number variations (CNV), and the first-line test in patients with GDD an...

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Bibliografiska uppgifter

Huvudupphov:	Beronja Branko, Đuranović Ana, Perović Dijana
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	University of Belgrade, Medical Faculty 2023-01-01
Serie:	Medicinski Podmladak
Ämnen:	copy number variation molecular karyotyping c15 developmental delay
Länkar:	https://scindeks-clanci.ceon.rs/data/pdf/0369-1527/2023/0369-15272305043B.pdf
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