Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the locus control region-Reference-Cited by-同舟云学术

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Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the locus control region

Published:2015-02-14 Issue:5 Volume:100 Page:e166-e168
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Amid A.,Cheong M.,Eng B.,Hanna M.,Hohenadel B.-A.,Nakamura L. M.,Walker L.,Odame I.,Kirby-Allen M.,Waye J. S.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 6 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. A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with Haemoglobinopathies;International Journal of Molecular Sciences;2022-12-14

2. RS12574989 and haplotype associated with α/β-chain imbalance and population HbA2 reduction;BMC Medical Genomics;2022-08-15

3. Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing;The Journal of Molecular Diagnostics;2021-12

4. The human β‐globin enhancer LCR HS2 plays a role in forming a TAD by activating chromatin structure at neighboring CTCF sites;The FASEB Journal;2021-05-25

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

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