DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Chen CP, Lin CJ, Chen YY. , et al.
3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.
Gene 2013;
532 (01) 80-86
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