ArticleBMC medical genomics2023
A case report: Marfan syndrome with X trisomy and FBN1 and SDHB mutations.
Jiansheng Lin et al.PubMed ↗Full text ↗Publisher ↗
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ArticleBMC medical genomics2023
Jiansheng Lin et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.