⌘+K

Pulse Explore Clubs Researchers Journals

Home Clubs Explore

August 10, 2024

[Genetic analysis of a fetus with with 45,X/46,X,idic(Y)(q11.2) mosaicism].

Feiyan Pan Weiqing Zhang Weiguo Zhang

View Full Paper

Ask AI

Bookmark

Share

Abstract

To explore the genetic characteristics of a fetus with sex chromosome abnormality indicated by non-invasive prenatal testing (NIPT) at 25

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Pan et al. (2024) studied this question.

synapsesocial.com/papers/68e5cc6bb6db643587562c79 https://doi.org/10.3760/cma.j.cn511374-20230807-00042

View Full Paper

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Case Report: Prenatal genetic analysis of a rare fetus with 45, X/46, X, dic r (Y; Y)/46, X, r(Y) karyotypeCase Report · 2026
2Prenatal diagnosis, genetic analysis, and pregnancy outcomes of fetuses with mosaic isodicentric Y chromosomesOriginal Research · 2026
3Using SNP microarray to distinguish mosaicism from chimerism in a phenotypically normal male newborn with prenatal 46,XX/46,XY karyotypeOriginal Research · 2026
4High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with perinatal progressive decrease of the 45,X cell line, a favorable fetal outcome and the karyotype of 45,X/47,XXX/46,XX in the neonate's peripheral blood at age 11 monthsOriginal Research · 2026
5[A case of mosaicism involving trisomy 21, maternal uniparental isodisomy, and normal diploid cells: Challenges and reflections in prenatal diagnosis].2025