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10 merged results for "Aneuploidy Screening"

Partial results: at least one source did not answer. Available results are shown rather than treating an upstream outage as zero matches.

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  1. Fetal Cells in Maternal Blood for Noninvasive Prenatal Testing-Is it Still a Distant Star?

    Singh R, Ravn K, Jeppesen LD, Laursen MB · 2026 · Prenatal diagnosis

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1002/pd.70304

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  2. CT- and MRI-detected calcification to predict 1p/19q codeletion status in gliomas: a systematic review and meta-analysis.

    Raposo-Neto JJ, de Almeida GC, Guimarães IM, Dias EL · 2026 · BMC cancer

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1186/s12885-026-16730-8

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  3. Non-invasive prenatal testing - new possibilities on the horizon and old problems.

    Weise A, Liehr T · 2026 · Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.1515/medgen-2026-3028

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  4. Causes of discordance between noninvasive prenatal testing and fetal chromosomal status: a 10-year cohort study of 97, 743 cases.

    Qi H, Chen H, Yuan X, Gan J · 2026 · Frontiers in endocrinology

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.3389/fendo.2026.1945762

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  5. Prenatal diagnostic outcomes and positive predictive values in 1,326 pregnancies with high-risk non-invasive prenatal testing results.

    Du R, Zhao B, Shi X, Gao Y · 2026 · Frontiers in genetics

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.3389/fgene.2026.1899719

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    • not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  6. Recurrent CNVs in constitutional CMA: a ClinGen-anchored single-center postnatal and prenatal experience.

    Satkın NB, Atlı E, Yalcintepe S, Çelik KM · 2026 · Frontiers in genetics

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.3389/fgene.2026.1960791

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  7. [Genetic analysis of two patients with isodicentric Y chromosomes].

    Yan J, Lin J, Yan Y, Lin Y · 2026 · Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.3760/cma.j.cn511374-20251223-00742

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  8. [Predictive value of maternal age, AMH level, and number of PGT cycles for the acquisition of euploid blastocysts: Construction and validation of a Nomogram model].

    Tan C, Wang X, Zou P, Fei J · 2026 · Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.3760/cma.j.cn511374-20260809-00360

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  9. Systematic analysis of genetic vulnerabilities caused by chromosome loss events in cancer.

    Bei Y, Keane J, Lynch M, Tamaru KM · 2026 · bioRxiv : the preprint server for biology

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.64898/2026.10.26.762060

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  10. Preimplantation Genetic Testing for Aneuploidy: A Health Technology Assessment.

    Ontario Health, Ontario Health · 2026 · Ontario health technology assessment series

    uncertain Transparent signal score 50/100 · policy 1.0.0

    Found in pubmed · no DOI

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer