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

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

Abstract 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...

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Bibliographic Details
Main Authors: Li Gao, Junyu Zhang, Xu Han, Wenjing Hu, Jinling Sun, Yuru Tan, Xinrong Zhao, Renyi Hua, Shan Wang, Yan Zhang, Yanlin Wang, Yi Wu
Format: Article
Language:English
Published: BMC 2020-11-01
Series:Molecular Cytogenetics
Subjects:
1p36 deletion syndrome
Prenatal diagnosis
Isolated dextrocardia
Chromosomal microarray analysis
Whole genome sequencing
Online Access:http://link.springer.com/article/10.1186/s13039-020-00514-1

Internet

http://link.springer.com/article/10.1186/s13039-020-00514-1

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