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Article

Weill-Marchesani-like syndrome caused by an FBN1 mutation with low-penetrance.

Chinese medical journal - 23 Mar 2021

Yang Guo-Yuan, Huang Xi, Chen Bing-Jie, Xu Zhu-Ping

Abstract excerpt

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Topics

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Dwarfism
Eye Diseases, Hereditary
Fibrillin-1
Mutation
Pedigree
Penetrance
Syndrome

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Identifiers

PMID: 34075901
DOI: 10.1097/CM9.0000000000001406
PMCID: PMC8183799

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