← Evidence map

ArticleMolecular genetics & genomic medicine2019

Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families.

Bo Gong et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

4 papers cite it

2019
2020
2021
2022
2023
2024
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 30838813