Prenatal Screening Via cfDNA – Paired‐End Sequencing Utilizing Fragment Size Information Reduces the Screen Positive Rate for X Chromosome Aneuploidies
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Wiley Open Access
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| Autori principali: | Susan Hancock, Franchesca Liao, Theresa Boomer, Sung Kim, Eileen de Feo |
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| Natura: | Artículo Open Access |
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Wiley
2026
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Documenti analoghi
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Correspondence on “Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use”
di: Julia Wynn, et al.
Pubblicazione: (2024) -
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Pubblicazione: (2025) -
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Pubblicazione: (2025) -
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