Molecular Characterization of α-Thalassemia in Adana, Turkey: A Single Center Study

Publisher： Karger

E-ISSN： 1421-9662|123|4|197-200

ISSN： 0001-5792

Source： Acta Haematologica, Vol.123, Iss.4, 2010-03, pp. : 197-200

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

α⁰-Thalassemia and Related Disorders in Northeast Thailand: A Molecular and Hematological Characterization

By  

Acta Haematologica, Vol. 117, Iss. 2, 2006-11 ,pp. : 78-82

Karger

Access to resources Recommend Favorite

α-Thalassemia in the United Arab Emirates

By  

Acta Haematologica, Vol. 100, Iss. 1, 1998-08 ,pp. : 49-53

Karger

Access to resources Recommend Favorite

The deferiprone and deferasirox combination is efficacious in iron overloaded patients with β‐thalassemia major: A prospective, single center, open‐label study

By  

PEDIATRIC BLOOD & CANCER (ELECTRONIC), Vol. 62, Iss. 9, 2015-09 ,pp. : 1592-1596

John Wiley & Sons Inc

Access to resources Recommend Favorite

Influence of α-Thalassemia on Cholelithiasis in SS Patients with Elevated Hb F

By  

Acta Haematologica, Vol. 100, Iss. 3, 1998-12 ,pp. : 147-150

Karger

Access to resources Recommend Favorite

Homozygous α-Thalassemia-1 Presenting in a Fetus without Anemia

By  

Acta Haematologica, Vol. 123, Iss. 4, 2010-04 ,pp. : 207-209

Karger

Access to resources Recommend Favorite