A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics

BACKGROUND: Array-based comparative genomic hybridization possesses a number of significant advantages over conventional cytogenetic and other molecular cytogenetic techniques, providing a sensitive and comprehensive detection platform for unexpected imbalances in the genome wide. CASE PRESENTATION:...

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Hlavní autoři: Yin, Aihua, Lu, Jian, Liu, Chang, Guo, Li, Wu, Jing, Mai, Mingqin, Zhong, Yanfang, Zhang, Xiaozhuang
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2014
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4005634/
https://ncbi.nlm.nih.gov/pubmed/24735551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-7-26
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