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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
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 |
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