Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Splenomegaly and HBB[original query] |
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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 |
[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 |
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 |
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 |
A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as ?-Thalassemia Intermedia Due to a KLF1 Gene Mutation. Hemoglobin 2019 6 43 (2): 140-144. Yang Kun, Ren Quan, Wu Yi, Zhou Yali, Yin Xiaol |
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