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Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome
Authors:Patrick K. C. Au  Yvonne K. Y. Kwok  K. Y. Leung  Linda Y. F. Tang  Mary H. Y. Tang  Elizabeth T. Lau
Affiliation:1. Prenatal Diagnostic and Counselling Department, Tsan Yuk Hospital, Hong Kong, China

Department of Medicine, The University of Hong Kong, Hong Kong, China;2. Department of Obstetrics and Gynaecology, The University of Hong Kong, Hong Kong, China;3. Prenatal Diagnostic and Counselling Department, Tsan Yuk Hospital, Hong Kong, China

Abstract:
Keywords:Apert syndrome  molecular beacon  plasma DNA  non-invasive prenatal diagnosis
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