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.

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@article{Chen2012IdentificationOA, title={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.}, author={Chih-Ping Chen and Yi-Ning Su and Fang-Yu Hung and S H Chern and Jun-Wei Su and Wayseen Wang}, journal={Taiwanese journal of obstetrics & gynecology}, year={2012}, volume={51 2}, pages={312-4} }