Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients

BACKGROUND: Array‐based genomic analysis is a gold standard for the detection of copy number variations (CNVs) as an important source of benign as well as pathogenic variations in humans. The introduction of chromosomal microarray (CMA) has led to a significant leap in diagnostics of genetically cau...

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Detalles Bibliográficos
Autores principales: Perovic, Dijana, Damnjanovic, Tatjana, Jekic, Biljana, Dusanovic‐Pjevic, Marija, Grk, Milka, Djuranovic, Ana, Rasic, Milica, Novakovic, Ivana, Maksimovic, Nela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169173/
https://www.ncbi.nlm.nih.gov/pubmed/35441737
http://dx.doi.org/10.1002/jcla.24441

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169173/
https://www.ncbi.nlm.nih.gov/pubmed/35441737
http://dx.doi.org/10.1002/jcla.24441

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