Na Ma
3PUBLICATIONS
5CO-AUTHORS
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Publications (3)
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|Jul 22, 2021
Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.Jing Liu, Qin Liu, Shuting Yang
|Apr 09, 2021
Clinical and genetic analysis of classical Ehlers-Danlos syndrome patient caused by synonymous mutation in COL5A2.Na Ma, Zhenhua Zhu, Jing Liu
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