Sickle cell trait knowledge and health literacy in caregivers who receive in-person sickle cell trait education

Author:

Creary Susan1ORCID,Adan Ismahan1,Stanek Joseph1,O'Brien Sarah H.1,Chisolm Deena J.1,Jeffries Tanica1,Zajo Kristin1,Varga Elizabeth1

Affiliation:

1. Nationwide Children's Hospital; Columbus Ohio

Funder

Foundation for the National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Reference21 articles.

1. Elk Grove Village, IL. Serving the family from birth to the medical home. Newborn screening: a blueprint for the future - a call for a national agenda on state newborn screening programs;AAP Newborn Screening Task Force;Pediatrics,2000

2. Interventions for patients and caregivers to improve knowledge of sickle cell disease and recognition of its related complications;Asnani;Cochrane Data. Syst. Rev.,2016

3. Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment;Bernhardt;Am. J. Med. Genet.,2000

4. Centers for Disease Control Data and Statistics https://www.cdc.gov/ncbddd/sicklecell/data.html

5. Incidence of sickle cell trait - United States, 2010, 2014;Centers for Disease Control and Prevention;Morb. Mortal. Wkly Rep.,2014

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