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1p36 deletion syndrome,Prenatal diagnosis,Isolated dextrocardia,Chromosomal microarray analysis,Whole genome sequencing
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BioMed Central
Molecular Cytogenetics, https://doi.org/10.1186/s13039-020-00514-1
1p36 deletion syndrome
Prenatal diagnosis
Isolated dextrocardia
Chromosomal microarray analysis
Whole genome sequencing
A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report
Li Gao
Junyu Zhang
Xu Han
Wenjing Hu
Jinling Sun
Yuru Tan
Xinrong Zhao
Renyi Hua
Shan Wang
Yan Zhang
Yanlin Wang
Yi Wu
10.1186/s13039-020-00514-1
2010-04-23
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Molecular Cytogenetics
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2010-04-23
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