ArticleNPJ genomic medicine2022
Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders.
Sen Zhao et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
25 papers cite it
this papercites it
ArticleNPJ genomic medicine2022
Sen Zhao et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.