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Lin, S. et al. (2018). Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions. Prenatal diagnosis. pp. 381-389. [Online].
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Lin, S. et al. (2018). Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions. Prenatal diagnosis. pp. 381-389. [Online].