{"identifier":"nobleid:/w1/20260526/2F373C39","arkIdentifier":"ark:/48914/w1/20260526/2F373C39","version":1,"workTitle":"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.","workType":"Journal Article","authors":"Numbere N, Weber DR, Porter G Jr, Iqbal MA","description":null,"workUrl":null,"existingDoi":"10.1002/mgg3.1241","createdAt":"2026-05-26T03:10:46.639247Z","canonicalUrl":"https://nobleid.org/ark:/48914/w1/20260526/2F373C39.v1"}