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Genomics‐based non‐invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women
BACKGROUND: Common fetal aneuploidies include Down syndrome (trisomy 21 or T21), Edward syndrome (trisomy 18 or T18), Patau syndrome (trisomy 13 or T13), Turner syndrome (45,X), Klinefelter syndrome (47,XXY), Triple X syndrome (47,XXX) and 47,XYY syndrome (47,XYY). Prenatal screening for fetal aneup...
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| Publicado no: | Cochrane Database Syst Rev |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Ltd
2017
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6486016/ https://ncbi.nlm.nih.gov/pubmed/29125628 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD011767.pub2 |
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