ArticleOrphanet journal of rare diseases2022
Delineation of dual molecular diagnosis in patients with skeletal deformity.
Lian Liu et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleOrphanet journal of rare diseases2022
Lian Liu et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.