Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients-Reference-Cited by-同舟云学术

Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients

Published:2009-09 Issue:9 Volume:84 Page:603-606
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Koenig Sara C.,Becirevic Esmira,Hellberg Miriam S.C.,Li Michael Y.,So Jason C.C.,Hankins Jane S.,Ware Russell E.,McMahon Lillian,Steinberg Martin H.,Luo Hong-Yuan,Chui David H.K.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.21480/fullpdf

Reference24 articles.

1. β-Globin regulation and long-range interactions;Palstra;Adv Genet,2008

2. DNA sequence variation associated with elevated fetal Gγ globin production;Gilman;Blood,1985

3. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb β-globin gene deletion;Andersson;Eur J Haematol,2006

4. The human β-globin locus control region;Levings;Eur J Biochem,2002

Cited by 15 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. The carrier state for sickle cell disease is not completely harmless;Haematologica;2019-05-16

2. SIRT1activates the expression of fetal hemoglobin genes;American Journal of Hematology;2017-08-28

3. Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease;Advances in Experimental Medicine and Biology;2017

4. Loss of Major DNase I Hypersensitive Sites in Duplicatedβ-globinGene Cluster Incompletely SilencesHBBGene Expression;Human Mutation;2016-08-25

5. Diverse hematological phenotypes of β-thalassemia carriers;Annals of the New York Academy of Sciences;2016-03