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Expanding Access to Noninvasive Prenatal Diagnosis for Monogenic Conditions to Consanguineous Families.
- Published in:
- Clinical Chemistry, 2024, v. 70, n. 5, p. 727, doi. 10.1093/clinchem/hvae023
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- Article
Noninvasive Prenatal Diagnosis of Single-Gene Diseases: The Next Frontier.
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- Clinical Chemistry, 2020, v. 66, n. 1, p. 53, doi. 10.1373/clinchem.2019.304238
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- Article
Non-invasive prenatal diagnosis (NIPD): how analysis of cell-free DNA in maternal plasma has changed prenatal diagnosis for monogenic disorders.
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- Clinical Science, 2022, v. 136, n. 22, p. 1615, doi. 10.1042/CS20210380
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- Article
Non‐invasive fetal genotyping for maternal alleles with droplet digital PCR: A comparative study of analytical approaches.
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- Prenatal Diagnosis, 2023, v. 43, n. 4, p. 477, doi. 10.1002/pd.6333
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- Article
Lessons learnt from prenatal exome sequencing.
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- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 831, doi. 10.1002/pd.6165
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- Article
Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis.
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- Prenatal Diagnosis, 2022, v. 42, n. 6, p. 662, doi. 10.1002/pd.6115
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- Article