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A significant proportion of children of African descent with HbSß0 thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.
Day, Melissa E; Rodeghier, Mark; Driggers, Jennifer; Bean, Christopher J; Volanakis, Emmanuel J; DeBaun, Michael R.
  • Day ME; Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Rodeghier M; Rodeghier Consultants, Chicago, IL, USA.
  • Driggers J; Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Bean CJ; Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Volanakis EJ; Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN, USA.
  • DeBaun MR; Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN, USA.
Br J Haematol ; 185(1): 153-156, 2019 04.
Article en En | MEDLINE | ID: mdl-29797315
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Talasemia beta / Errores Diagnósticos / Anemia de Células Falciformes Tipo de estudio: Diagnostic_studies Límite: Child / Humans País como asunto: Africa Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Talasemia beta / Errores Diagnósticos / Anemia de Células Falciformes Tipo de estudio: Diagnostic_studies Límite: Child / Humans País como asunto: Africa Idioma: En Año: 2019 Tipo del documento: Article