Taiwanese Journal of Obstetrics & Gynecology (Jun 2012)

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

  • Chih-Ping Chen,
  • Yi-Ning Su,
  • Fang-Yu Hung,
  • Schu-Rern Chern,
  • Jun-Wei Su,
  • Wayseen Wang

DOI
https://doi.org/10.1016/j.tjog.2012.04.031
Journal volume & issue
Vol. 51, no. 2
pp. 312 – 314

Abstract

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