ArticleMolecular genetics & genomic medicine2020

A 235 Kb deletion at 17q21.33 encompassing the COL1A1, and two additional secondary copy number variants in an infant with type I osteogenesis imperfecta: A rare case report.

Numbereye Numbere et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.