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Clinical value for the detection of fetal chromosomal deletions/duplications by noninvasive prenatal testing in clinical practice
OBJECTIVE: This study was to report the experiences on the clinical value of noninvasive prenatal testing (NIPT) for the screening of fetal chromosomal deletions/duplications. METHODS: We performed a retrospective analysis of a cohort of 20,439 pregnancies undergoing NIPT from March 2017 to Septembe...
Tallennettuna:
| Julkaisussa: | Mol Genet Genomic Med |
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| Päätekijät: | , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8222853/ https://ncbi.nlm.nih.gov/pubmed/33951332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1687 |
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