Prenatal Diagnosis and Molecular Cytogenetic Characterization of Copy Number Variations on 4p15.2p16.3, Xp22.31, and 12p11.1q11 in a Fetus with Ultrasound Anomalies: A Case Report and Literature Review

Chromosomal rearrangements, such as duplications/deletions, can lead to a variety of genetic disorders. Herein, we reported a prenatal case with right aortic arch and aberrant left subclavian artery, consisting of a complex chromosomal copy number variations. Routine cytogenetic analysis described t...

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Dettagli Bibliografici
Pubblicato in:Biomed Res Int
Autori principali: Zhang, Han, Xi, Qi, Liu, Xiangyin, Yue, Fagui, Zhang, Hongguo, Sun, Meiling, Liu, Ruizhi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi 2020
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7275220/
https://ncbi.nlm.nih.gov/pubmed/32566663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/1761738
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