1. 
   Alpha thalassemia
   Our Alpha thalassemia Main Article provides a comprehensive look at the who, what, when and how of Alpha thalassemia Alpha thalassemia: A blood disorder, thalassemia is not one disease but rather a group of disorders that have a single feature in common: they all have a genetic defect in the product...
   Found op http://www.medterms.com/script/main/art.html?articlekey=7471
   
   
2. 
   Alpha-thalassemia
   Alpha-thalassemia (α-thalassemia) is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. The degree of impairment is based on which clinical phenotype is pre...
   Found op http://en.wikipedia.org/wiki/Alpha-thalassemia
   
   
3. 
   alpha-thalassemia
   α-thalassemia thalassemia caused by diminished synthesis of alpha chains of hemoglobin. The homozygous form is incompatible with life, the stillborn infant displaying severe hydrops fetalis. The heterozygous form may be asymptomatic or marked by mild anemia.
   Found op http://www.encyclo.co.uk/local/21001
   
   
4. 
   alpha-thalassemia
   (from the article `blood disease`) The defect in thalassemia may involve the -chains of globin (-thalassemia), the -chains (-thalassemia), the -chains (-thalassemia), or both - and ... ...inheritance, a few (such as the two heterozygous -thalassemias) are benign and generally exhibit no clinical sym...
   Found op http://www.britannica.com/eb/a-z/a/52
   
   

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