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Query Trace: Splenomegaly and HBB[original query]

Hb E-ß-Thalassemia in Five Indian States. Hemoglobin 2016 Sep 1-6. Italia Khushnooma, Dabke Pooja, Sawant Pratibha, Nadkarni Anita, Ghosh Kanjaksha, Colah Roshan Similar articles in PubMed
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) ß(0) -thalassaemia homozygotes. British journal of haematology 2016 Jan . Jiang Zhihua, Luo Hong-Yuan, Huang Shengwen, Farrell John J, Davis Lance, Théberge Roger, Benson Katherine A, Riolueang Suchada, Viprakasit Vip, Al-Allawi Nasir A S, Ünal Sule, Gümrük Fatma, Akar Nejat, Ba?ak A Nazli, Osorio Leonor, Badens Catherine, Pissard Serge, Joly Philippe, Campbell Andrew D, Gallagher Patrick G, Steinberg Martin H, Forget Bernard G, Chui David H Similar articles in PubMed
[Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series]. Archivos argentinos de pediatría 2015 Oct 113 (5): e294-8. Eandi Eberle Silvia, Pepe Carolina, Aguirre Fernando, Milanesio Berenice, Fernández Diego, Mansini Adrián, Chávez Alejandro, Sciuccati Gabriela, Díaz Lilian, Candás Andrea, Avalos Gómez Vanesa, Bonduel Mariana, Feliú Torres Auro Similar articles in PubMed
Molecular update of ß-thalassemia mutations in the Syrian population: identification of rare ß-thalassemia mutations. Hemoglobin 2014 38 (4): 272-6. Jarjour Rami A, Murad Hossam, Moasses Faten, Al-Achkar Wal Similar articles in PubMed