Literature DB >> 20147853

A case of mild thalassemic syndrome caused by interaction of Hb Adana with an alpha+-thalassemia deletion.

Marina Economou, Economou Marina, Eleni Papadopoulou, Papadopoulou Eleni, Ioanna Tsatra, Tsatra Ioanna, Miranda Athanassiou-Metaxa, Athanassiou-Metaxa Miranda.   

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Year:  2010        PMID： 20147853     DOI： 10.1097/MPH.0b013e3181c5ab89

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN： 1077-4114            Impact factor:   1.289


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  2 in total

1.  Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent.

Authors:  A Tampaki; S Theodoridou; Ch Apostolou; E E Delaki; E Vlachaki
Journal:  Hippokratia       Date:  2020 Jan-Mar       Impact factor: 0.471

2.  DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia.

Authors:  Jin Ai Mary Anne Tan; Siew Leng Kho; Chin Fang Ngim; Kek Heng Chua; Ai Sim Goh; Seoh Leng Yeoh; Elizabeth George
Journal:  Sci Rep       Date:  2016-06-08       Impact factor: 4.379
  2 in total

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