Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT - Chang, Jiazhen; Song, Yingna; Qi, Qingwei; Hao, Na; Liu, Juntao (Zhonghua yi xue yi chuan xue za zhi, 2023)
Keywords: Amniotic Fluid; Chromosome Aberrations; Chromosomes, Human, Pair 1; DNA Copy Number Variations; Female; Fetus; Humans; In Situ Hybridization, Fluorescence; Placenta; Pregnancy; Prenatal Diagnosis - methods; Trisomy - genetics; Trisomy 13 Syndrome - diagnosis; Trisomy 13 Syndrome - genetics