Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II
- Resource Type
- Article
- Source
- In
Taiwanese Journal of Obstetrics & Gynecology June 2012 51(2):312-314 - Subject
- Language
- ISSN
- 1028-4559