Dittrich T

No ORCID on file · 1 paper in corpus · active 2026
2026
Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicism.
Molecular cytogenetics ·doi:10.1186/s13039-026-00762-7

BackgroundPartial trisomy 21 is a rare chromosomal aberration that can provide unique insights into genotype-phenotype correlations in Down syndrome (DS). While non-invasive prenatal testing (NIPT) has become a widely used screening tool fo…