Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference25 articles.
1. Modulation of Fetal Hemoglobin Synthesis by Iron Deficiency
2. Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion
3. A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to ?-thalassemia
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1. Probability of high-risk genetic matching with oocyte and semen donors: complete gene analysis or genotyping test?;Journal of Assisted Reproduction and Genetics;2022-01-29
2. Genetic variants of HBS1L-MYB with Hb subtypes level among Filipino β°-deletion carriers co-inherited with −α3.7 deletion thalassaemia;Meta Gene;2020-12
3. Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene;Hemoglobin;2017-11-02
4. Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR);BMC Medical Genetics;2016-10-19
5. HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?;Pathology;2013-01
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