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

Affiliations

Chih-Ping Chen

Department of Medicine, Mackay Medical College, New Taipei City, Taiwan

Yi-Ning Su

Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan

Fang-Yu Hung

Department of Obstetrics and Gynecology, Mackay Memorial Hospital Hsinchu Branch, Hsinchu, Taiwan

Schu-Rern Chern

Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan

Jun-Wei Su

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan

Wayseen Wang

Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan