Diagnosis of the accurate genotype of HKαα carriers in patients with thalassemia using multiplex ligation-dependent probe amplification combined with nested polymerase chain reaction-Reference-Cited by-同舟云学术

Diagnosis of the accurate genotype of HKαα carriers in patients with thalassemia using multiplex ligation-dependent probe amplification combined with nested polymerase chain reaction

Published:2020-04-21 Issue:10 Volume:133 Page:1175-1181
ISSN:0366-6999
Container-title:Chinese Medical Journal
language:en
Short-container-title:

Author:

Chen Dong-Mei,Ma Shi,Tang Xiang-Lan,Yang Ji-Yun,Yang Zheng-Lin

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,General Medicine

Reference24 articles.

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3. Molecular epidemiological investigation of thalassemia in the Chengdu Region, Sichuan Province, Southwest China;Yu;Hemoglobin,2015

4. Unusual rearrangement of the alpha-globin gene cluster containing both the -alpha3.7 and alphaalphaalphaanti-4.2 crossover junctions: clinical diagnostic implications and possible mechanisms;Wang;Clin Chem,2005

5. Molecular characterization and clinical presentation of HKαα and anti-HKαα alleles in southern Chinese subjects;Shang;Clin Genet,2013

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