Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait

Genetic Epidemiology and Preventive Healthcare in Multiethnic Societies: The Hemoglobinopathies

(2014) Piero Giordano et al.   International Journal of Environmental Research and Public Health

Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000

(2014) Frédéric B Piel et al.   Lancet Global Health

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

(2013) Belinda Giardine et al.   NUCLEIC ACIDS RESEARCH

World Distribution, Population Genetics, and Health Burden of the Hemoglobinopathies

(2013) T. N. Williams et al.   Cold Spring Harbor Perspectives in Medicine

β-Globin chain abnormalities with coexisting α-thalassemia mutations

(2012) Birol Guvenc et al.   Archives of Medical Science

The triumph of good over evil: protection by the sickle gene against malaria

(2012) H. F. Bunn   BLOOD

Differing effects of HbS and HbC traits on uncomplicated falciparum malaria, anemia, and child growth

(2010) B. Kreuels et al.   BLOOD

The inherited diseases of hemoglobin are an emerging global health burden

(2010) D. J. Weatherall   BLOOD

Significant haemoglobinopathies: guidelines for screening and diagnosis

(2010) Kate Ryan et al.   BRITISH JOURNAL OF HAEMATOLOGY

Implementation of the newborn screening programme for sickle cell disease in England: results for 2003-2005

(2008) Allison Streetly et al.   JOURNAL OF MEDICAL SCREENING