Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations-Reference-Cited by-同舟云学术

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Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations

Published:1992 Issue:2-3 Volume:88 Page:82-85
ISSN:0001-5792
Container-title:Acta Haematologica
language:en
Short-container-title:Acta Haematol

Author:

Fei You-Jun,Öner Reyhan,Bözkurt Gulsen,Gu Li-Hao,Altay Çigdem,Gurgey Aytemiz,Fattoum Slaheddine,Baysal Erol,Huisman Titus H.J.

Publisher

S. Karger AG

Subject

Hematology,General Medicine

Cited by 26 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. Hemoglobin H hastalığında genetik danışmanlık önemli midir?;Cukurova Medical Journal;2023-07-02

2. Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran;Scientific Reports;2022-03-22

3. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region;Hemoglobin;2020-01-02

4. Molecular and geographical heterogeneity of hemoglobinopathy mutations in Azerbaijanian populations;Annals of Human Genetics;2019-11-21

5. Genetics of Iranian Alpha-Thalassemia Patients: A Comprehensive Original Study;Biochemical Genetics;2018-04-07

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