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Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience

Chromosomal microarray analysis (CMA) is now established as the first-tier cytogenetic diagnostic test for fast and accurate detection of chromosomal abnormalities in patients with developmental delay/intellectual disability (DD/ID), multiple congenital anomalies (MCA), and autism spectrum disorders...

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Detalhes bibliográficos
Main Authors: Žilina, Olga, Teek, Rita, Tammur, Pille, Kuuse, Kati, Yakoreva, Maria, Vaidla, Eve, Mölter-Väär, Triin, Reimand, Tiia, Kurg, Ants, Õunap, Katrin
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Periodicals, Inc. 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3960059/
https://ncbi.nlm.nih.gov/pubmed/24689080
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.57
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