Niscola, Pasquale <br/><br/>
Diagnosis of myelodysplastic syndromes in individuals heterozygous for mutations in the α- and β-globin genes: a reminder for haematologists.  [electronic resource] 

 -  Blood transfusion = Trasfusione del sangue  Jan 2014 
 - s158-9 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>2385-2070 
<br/><br/><label>Standard No.: </label>10.2450/2013.0083-13  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Asymptomatic Diseases<br/>Blood Transfusion<br/>Bone Marrow--pathology<br/>Delayed Diagnosis<br/>Diagnosis, Differential<br/>Erythropoiesis<br/>Erythropoietin--therapeutic use<br/>Female<br/>Follow-Up Studies<br/>Hemoglobins--analysis<br/>Heterozygote<br/>Humans<br/>Incidental Findings<br/>Male<br/>Myelodysplastic Syndromes--diagnosis<br/>Phenotype<br/>Thalassemia--diagnosis<br/>alpha-Globins--genetics<br/>beta-Globins--genetics