Identification of patients with defects in the globin genes

INTRODUCTION: hemoglobinopathies constitute a major health problem worldwide. These disorders are characterized by a clinical and hematological phenotypic heterogeneity. The increase of HbA2 is an invaluable hematological marker of the beta-thalassemia heterozygosis and of double heterozygosis for t...

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Veröffentlicht in:Journal of prenatal medicine. - 2007. - 7(2013), 4 vom: 20. Okt., Seite 47-50
1. Verfasser: Dell'edera, Domenico (VerfasserIn)
Weitere Verfasser: Epifania, Annunziata Anna, Milazzo, Giusi Natalia, Leo, Manuela, Santacesaria, Carmela, Allegretti, Arianna, Mazzone, Eleonora, Panetta, Paolo, Iammarino, Giovanna, Lupo, Maria Giovanna, Barbieri, Rocchina, Lioi, Maria Brigida
Format: Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Journal of prenatal medicine
Schlagworte:Case Reports Journal Article HbA2 borderline carrier screening prenatal diagnosis β-thalassemia