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Prenatal screening for congenital anomalies: exploring midwives’ perceptions of counseling clients with religious backgrounds
BACKGROUND: In the Netherlands, prenatal screening follows an opting in system and comprises two non-invasive tests: the combined test to screen for trisomy 21 at 12 weeks of gestation and the fetal anomaly scan to detect structural anomalies at 20 weeks. Midwives counsel about prenatal screening te...
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| Publicat a: | BMC Pregnancy Childbirth |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4223558/ https://ncbi.nlm.nih.gov/pubmed/25037919 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2393-14-237 |
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