Case report
Oct 2026
[Genetic analysis of two fetuses with supernumerary small marker chromosomes derived from complex chromosomal rearrangements].
Ch Chromosomal karyotyping combined with CNV-Seq can elucidate the size and genetic content of the sSMCs, thereby facilitating prenatal diagnosis and genetic counseling, and NIPT has value in screening for fetuses with sSMCs.
Fei-Yan Pan, Meizhen Dai, Yuan-Yuan Ying et al.
· Zhonghua yi xue yi chuan xue... · 0 citations