Haiyan Tang
3PUBLICATIONS
1CO-AUTHORS
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Publications (3)
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|Dec 17, 2021
Novel compound heterozygous mutations in the CYP4F22 gene in a patient with autosomal recessive congenital ichthyosis.Haiyan Tang, Xiaoliu Shi, Guiying Zhang
|Jul 29, 2021
Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified.Zhongyan Xiao, Yuan Yang, Hui Huang
|Jul 02, 2021
Novel homozygous protein-truncating mutation of BBS9 identified in a Chinese consanguineous family with Bardet-Biedl syndrome.Hai-Yan Tang, Fen Xie, Ru-Chun Dai
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