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BioMed Central, BMC Medical Genomics, 1(11), 2018

DOI: 10.1186/s12920-018-0409-z

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Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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