A mild type of Hb S-β+-thalassemia [-92(C→T)] in a sicilian family-Reference-Cited by-同舟云学术

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A mild type of Hb S-β+-thalassemia [-92(C→T)] in a sicilian family

Published:1993-02 Issue:2 Volume:42 Page:225-226
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Divoky V.,Baysal E.,Schiliro G.,Dibenedetto S. P.,Huisman T. H. J.

Publisher

Wiley

Subject

Hematology

Reference5 articles.

1. Molecular characterization of Hb S(C) β-thalassemia in American blacks

2. , , , , : Clinical, hematological, and molecular features in Sicilians with Hb S-β-thalassemia. Am J Hematol (in press).

3. Fetal hemoglobin in normal adults and ?-thalassemia heterozygotes

4. The β- and δ-Thalassemia Repository

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. First Report of β-Thalassemia Intermedia in a Patient Compound Heterozygous for –92 (C>T) and Codons 36/37 (–T) Mutations;Hemoglobin;2018-06-12

2. The regulation of human globin promoters by CCAAT box elements and the recruitment of NF-Y;Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms;2017-05

3. The compound state: Hb S/beta-thalassemia;Revista Brasileira de Hematologia e Hemoterapia;2015-05

4. Very mild forms of Hb S/beta+-thalassemia in Brazilian children;Revista Brasileira de Hematologia e Hemoterapia;2015-05

5. Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population;American Journal of Human Biology;2015-03-07

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