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Article

Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome

13 Jul 2022

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 35841934
DOI: 10.1016/j.ajog.2022.07.004

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Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndromePMID 35841934Read ↗

Non-Invasive Prenatal Testing by Cell-Free DNA (cfNIPT) for Detecting Turner Syndrome With Mosaicism and Structural Variants-Prenatal Findings and Postnatal Outcomes.Semantic proximity Read ↗

Diagnostic testing after positive results on cell free DNA screening: CVS or Amnio?Semantic proximity Read ↗

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Maternal cell-free DNA–based screening for fetal microdeletion and the importance of careful diagnostic follow-upSemantic proximity Read ↗

Turner SyndromeSemantic proximity Read ↗

Chromosome-selective sequencing of maternal plasma cell–free DNA for first-trimester detection of trisomy 21 and trisomy 18Semantic proximity Read ↗

Cell‐free DNA screening for rare autosomal trisomies and segmental chromosome imbalancesSemantic proximity Read ↗

Cytogenomic characterization of mosaic X-ring chromosomes in seventeen patients with Turner syndrome (TS)-42 years of experience at a single-site institution.Semantic proximity Read ↗

Cell-free fetal DNA versus maternal serum screening for trisomy 21 in pregnant women with and without assisted reproduction technology: a prospective interventional studySemantic proximity Read ↗

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicismSemantic proximity Read ↗

Implications of fetoplacental mosaicism on cell‐free DNA testing for sex chromosome aneuploidiesSemantic proximity Read ↗

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