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Meina Lin

2PUBLICATIONS

0CO-AUTHORS

Gene mappingCentral nervous system

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Publications (2)

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|Jan 18, 2021

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

Meina Lin, Ying Jin, Xinren Chen

|Jul 19, 2019

Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.

Meina Lin, Yongping Lu, Yu Sui

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