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Papoulidis, I., Oikonomidou, E., Orru, S., et al (2013) Prenatal Detection of TAR Syndrome in a Fetus with Compound Inheritance of an RBM8A SNP and a 334-kb Deletion: A Case Report. Molecular Medicine Reports, 9, 163-165.
https://doi.org/10.3892/mmr.2013.1788

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