X. Ni

A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A

M. Jiang, Y. Sui, Yong-ping Lu, 2021, BMC medical genomics.

A Milroy Disease Family Caused by FLT4 Gene Mutation of c.2774 T>A

M. Jiang, Y. Sui, Yong-ping Lu, 2020 .

A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease

M. Jiang, N. Zhao, Y. Sui, 2020, Ophthalmic genetics.

Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6–48 months with Duchenne muscular dystrophy amenable to exon 51 skipping

M. Pane, F. Muntoni, L. Servais, 2023, Neuromuscular Disorders.

Increased hydrophobicity of CRYGD p.(Ala159ProfsTer9): Suspected cause of congenital cataracts in a large Chinese family

M. Jiang, N. Zhao, Y. Sui, 2020, Molecular genetics & genomic medicine.

Growth factors in the treatment of Achilles tendon injury

Meina Lin, Xinren Chen, Huan Li, 2023, Frontiers in bioengineering and biotechnology.

Missense variants of FBN2 associated with congenital arachnodactyly in three Chinese families

Meina Lin, Xinren Chen, Huan Li, 2024, Molecular Genetics and Metabolism Reports.