Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis.
Andrea ŠtefekováPavlína ČapkováVáclava CurtisováEnghjargalan MrackáHana FilipováZuzana SpurnáMartin ProcházkaMarek ĽubuškýRadovan PilkaRadek VrtělPublished in: Ceska gynekologie (2023)
A higher success rate for the detection of pathological copy number variation variants by the microarray method than by the MLPA method was confirmed.