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HARVARD Citation
Shariati, G. et al. (2018). Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH. Clinical case reports. 6 (8), pp. 1464-1469. [Online].
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Shariati, G. et al. (2018). Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH. Clinical case reports. 6 (8), pp. 1464-1469. [Online].