Imparting carrier status results detected by universal newborn screening for sickle cell and cystic fibrosis in England: a qualitative study of current practice and policy challenges

BACKGROUND: Universal newborn screening for early detection of children affected by sickle cell disorders and cystic fibrosis is currently being implemented across England. Parents of infants identified as carriers of these disorders must also be informed of their baby's result. However there i...

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Detalles Bibliográficos
Autores principales: Parker, Hilda, Qureshi, Nadeem, Ulph, Fiona, Kai, Joe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235853/
https://www.ncbi.nlm.nih.gov/pubmed/18078504
http://dx.doi.org/10.1186/1472-6963-7-203

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235853/
https://www.ncbi.nlm.nih.gov/pubmed/18078504
http://dx.doi.org/10.1186/1472-6963-7-203

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