SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold - Kievskaya, J.K.; Shilova, N.V.; Kanivets, I.V.; Kudryavtseva, E.V.; Pyankov, D.V.; Korostelev, S.A. (Sovremennye tekhnologii v medit͡s︡ine, 2021)
Keywords: Clinical Supplements; DNA Copy Number Variations - genetics; Female; Fetus; Humans; Infant; Karyotype; Microarray Analysis; Nuchal Translucency Measurement; Pregnancy; Prenatal Diagnosis - methods; prenatal diagnostics; reciprocal translocation; DNA copies number variations; chromosomal microarray analysis; nuchal fold thickness