Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin

Providing Appropriate Genetic Information to Healthy Carriers of Hemoglobinopathy Can Be a Welcome and Safe Initiative: The Latium Example

(2012) Antonio Amato et al.   Genetic Testing and Molecular Biomarkers

Genetic modifiers of  -thalassemia and clinical severity as assessed by age at first transfusion

(2012) F. Danjou et al.   HAEMATOLOGICA

Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults

(2011) A. E. Gallienne et al.   HAEMATOLOGICA

ICSH recommendations for the measurement of Haemoglobin F

(2011) A. D. STEPHENS et al.   International Journal of Laboratory Hematology

Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations

(2009) P. VAN DELFT et al.   International Journal of Laboratory Hematology

Prevention strategies for severe hemoglobinopathies in endemic and nonendemic immigration countries: the Latium example

(2009) A. Amato et al.   PRENATAL DIAGNOSIS