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
oleh: Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier 2012-06-01 |
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