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Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening
BACKGROUND: Newborn screening (NBS) for sickle cell disease incidentally identifies heterozygous carriers of hemoglobinopathy mutations. In Ontario, Canada, these carrier results are not routinely disclosed, presenting an opportunity to investigate the potential health implications of carrier status...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMC Pediatr |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8247172/ https://ncbi.nlm.nih.gov/pubmed/34210267 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-021-02751-8 |
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