The 3? breakpoint of the Yunnanese ( A ???) 0 -thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the G ?-globin gene-Reference-Cited by-同舟云学术

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The 3? breakpoint of the Yunnanese ( A ???) 0 -thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the G ?-globin gene

Published:1998-07-29 Issue:1 Volume:103 Page:90-95
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Zhang Xue-Qing,Zhang J.-W.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050789.pdf

Cited by 18 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 5 kb Deletion in the β-Globin Gene Cluster Identified in a Chinese Patient;Hemoglobin;2022-07-04

2. 6q deletion is frequent but unrelated to patient prognosis in breast cancer;Breast Cancer;2021-10-08

3. First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family;Hemoglobin;2018-07-04

4. The prevalence and molecular characterization of (δβ)0-thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population;Journal of Clinical Laboratory Analysis;2017-08-01

5. Rapid Screening for Deleted Form of β-thalassemia by Real-Time Quantitative PCR;Journal of Clinical Laboratory Analysis;2016-08-16

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