‘It means everyone should know their status’: exploring lay conceptions of sickle cell trait and sickle cell trait screening among African Americans within middle reproductive age-Reference-Cited by-同舟云学术

‘It means everyone should know their status’: exploring lay conceptions of sickle cell trait and sickle cell trait screening among African Americans within middle reproductive age

Published:2017-02-21 Issue:7 Volume:23 Page:813-829
ISSN:1355-7858
Container-title:Ethnicity & Health
language:en
Short-container-title:Ethnicity & Health

Author:

Mayo-Gamble Tilicia L.¹^ORCID,Barnes Priscilla A.²,Cunningham Erves Jennifer³,Middlestadt Susan E.²,Lin Hsien-Chang²

Affiliation:

1. Department of Family and Community Medicine, Meharry Medical College, Nashville, USA

2. Department of Applied Health Science, Indiana University, Bloomington, USA

3. Department of Internal Medicine, Meharry Medical College, Nashville, USA

Publisher

Informa UK Limited

Subject

Public Health, Environmental and Occupational Health,Arts and Humanities (miscellaneous),Cultural Studies

Link

https://www.tandfonline.com/doi/pdf/10.1080/13557858.2017.1295135

Reference30 articles.

1. A Pilot Study to Explore Knowledge, Attitudes, and Beliefs about Sickle Cell Trait and Disease

2. Women with sickle cell trait: Reproductive decision-making

3. Screening and counselling for sickle cell disorders and thalassaemia: The experience of parents and health professionals

4. Sickle Cell Trait and Development of Microvascular Complications in Diabetes Mellitus

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3. (Lack of) knowledge of mothers about sickle cell trait and disease: a qualitative study;Revista Brasileira de Enfermagem;2022

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