Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs

• Váldodahkkit: Chih-Ping Chen (Dahkki), Shih-Shien Weng (Dahkki), Schu-Rern Chern (Dahkki), Shin-Wen Chen (Dahkki), Fang-Tzu Wu (Dahkki), Wayseen Wang (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Elsevier, 2021-05-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Objective: We present rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction (QF-PCR) analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly (HPE), ventricular septal defect (VSD), arthrogrypos...