Nainggolan, Ita M <br/><br/>
Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional α(+)-thalassemia mutations: diverse hematological and clinical features.  [electronic resource] 

 -  Hemoglobin  2013 
 - 297-305 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1532-432X 
<br/><br/><label>Standard No.: </label>10.3109/03630269.2013.775149  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Base Sequence<br/>Child<br/>Child, Preschool<br/>Epistasis, Genetic<br/>Female<br/>Genotype<br/>Hemoglobins, Abnormal--genetics<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant<br/>Male<br/>Molecular Sequence Data<br/>Multiplex Polymerase Chain Reaction<br/>Mutation<br/>Phenotype<br/>Sequence Deletion<br/>Severity of Illness Index<br/>alpha-Thalassemia--genetics