A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report

BACKGROUND: Chromosome 1p36 deletion syndrome is a contiguous genetic disorder with multiple congenital anomalies and mental retardation. It has been emerging as one of the most common terminal deletion syndromes in humans with the rapid utility of microarray analysis. However, the prenatal findings...

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Detalles Bibliográficos
Autores principales: Gao, Li, Zhang, Junyu, Han, Xu, Hu, Wenjing, Sun, Jinling, Tan, Yuru, Zhao, Xinrong, Hua, Renyi, Wang, Shan, Zhang, Yan, Wang, Yanlin, Wu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670715/
https://www.ncbi.nlm.nih.gov/pubmed/33292381
http://dx.doi.org/10.1186/s13039-020-00514-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670715/
https://www.ncbi.nlm.nih.gov/pubmed/33292381
http://dx.doi.org/10.1186/s13039-020-00514-1

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