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Case Reports

A Fetus with 17q23.1-q23.2 Microdeletion Presents with Primary Bilateral Lung Hypoplasia in Utero

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Pages 144-148 | Received 29 Mar 2022, Accepted 19 Apr 2022, Published online: 03 May 2022

Reference

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  • Karolak JA, Gambin T, Honey EM, Slavik T, Popek E, Stankiewicz P. A de novo 2.2 Mb recurrent 17q23.1q23.2 deletion unmasks novel putative regulatory non-coding SNVs associated with lethal lung hypoplasia and pulmonary hypertension: a case report. BMC Med Genomics. 2020;13(1):34. doi:10.1186/s12920-020-0701-6.
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