Meifang Zhao
3PUBLICATIONS
1CO-AUTHORS
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Publications (3)
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|Aug 02, 2025
A Novel LAMA2 Mutation (c.7412G>A) Was Found in a Chinese Patient With Congenital Muscular Dystrophy.Meifang Zhao, Yuxing Liu, Liangliang Fan
|Feb 10, 2025
A Novel Pathogenic Splicing Mutation of OFD1 is Responsible for a Boy with Joubert Syndrome Exhibiting Orofaciodigital Spectrum Anomalies, Polydactyly and Retinitis Pigmentosa.Liang Chen, Mei-Fang Zhao, Hui-Wen Deng
|May 03, 2024
A de novo Mutation (p.Gln277X) of Cyclin D2 is Responsible for a Child with Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome.Mei-Fang Zhao, Song-Lin Zhang, YangZiYu Xiang
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