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Xue-Jiao Chen

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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. · 0 citations

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