ArticleJournal of human genetics2020
Identification of novel FBN1 variations implicated in congenital scoliosis.
Mao Lin et al.PubMed ↗Full text ↗Publisher ↗
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ArticleJournal of human genetics2020
Mao Lin et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.