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Karyotypic and Molecular Genetic Changes Associated With Fetal Cardiovascular Abnormalities: Results of a Retrospective 4-Year Ultrasonic Diagnosis Study

Objective: To investigate the incidence of aneuploidy in fetuses with congenital heart defects (CHDs) and to further identify submicroscopic changes and global DNA methylation levels as potential biomarkers in complex CHD cases. Methods: Fetuses at high risk for birth defects or with obvious sonogra...

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Detalles Bibliográficos
Autores principales: Bao, Bihui, Wang, Yu, Hu, Hua, Yao, Hong, Li, Yuyan, Tang, Shuai, Zheng, Lihong, Xu, Yan, Liang, Zhiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654495/
https://www.ncbi.nlm.nih.gov/pubmed/23678296
http://dx.doi.org/10.7150/ijbs.5404