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Hemoglobin|November 9, 2016
Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia PhenotypePatrick G Gallagher, Yelena Maksimova, Vincent P Schulz, et al.
Hemoglobin|October 10, 2009
Iron chelation therapy for patients with myelodysplastic syndromeSu-Peng Yeh, Yang-Sheng Yang, Chao-Yuan Yao, et al.
Hemoglobin|October 10, 2009
Treatment with deferiprone for iron overload alleviates bone marrow failure in a Fanconi anemia patientYu-Hsiang Chang, Chen-Fu Shaw, Kang-Hsi Wu, et al.
Hemoglobin|January 1, 1987
Hb F-Xinjiang or A gamma T25(B7)Gly----Arg: a new slow-moving unstable fetal hemoglobin variantH Hu, M Ma
Hemoglobin|March 8, 2014
A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2Mohamed S M Khalil, Samy Marouf, David Element, et al.
Hemoglobin|March 12, 2014
Oxidation status of β-thalassemia minor and Hb H disease, and its association with glycerol lysis time (GLT50)Chris Adhiyanto, Yukio Hattori, Yasuhiro Yamashiro, et al.
Hemoglobin|January 1, 1987
Hyperunstable hemoglobin Toyama [alpha 2 136(H19)Leu----Arg beta 2]: detection and identification by in vitro biosynthesis with radioactive amino acidsY Ohba, K Yamamoto, Y Hattori, et al.
Hemoglobin|March 14, 2019
Identification of a Novel 9.7 kb Deletion Causing α0-Thalassemia in Two Pregnant Women in Southern ChinaLi Lin, Qi Yang, Shujie Zhang, et al.
Hemoglobin|July 25, 2019
A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De NovoKazi N Hasan, Abu Sufian, Ashish K Mazumder, et al.
Hemoglobin|April 11, 2017
The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, IranMasoumeh Jalilian, Farid Azizi Jalilian, Leila Ahmadi, et al.
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