Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot

• Váldodahkkit: Chih-Ping Chen (Dahkki), Chen-Yu Chen (Dahkki), Schu-Rern Chern (Dahkki), Peih-Shan Wu (Dahkki), Yen-Ni Chen (Dahkki), Shin-Wen Chen (Dahkki), Li-Feng Chen (Dahkki), Chien-Wen Yang (Dahkki), Wayseen Wang (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Elsevier, 2016-04-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Objective: To present prenatal diagnosis and molecular cytogenetic characterization of a de novo 15q14 microdeletion associated with tetralogy of Fallot (TOF). Materials and methods: This was the first pregnancy of a 31-year-old primigravid woman. The pregnancy was uneventful until 23 weeks of gesta...