Hb Q-Thailand heterozygosity unlinked with the (–α <sup>4.2</sup> /) α <sup>+</sup> -thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses-Reference-Cited by-同舟云学术

Hb Q-Thailand heterozygosity unlinked with the (–α ^4.2 /) α ⁺ -thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses

Published:2023-03-03 Issue:1 Volume:28 Page:
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Qin Danqing¹²³,Wang Jicheng¹²³,Yao Cuize¹²³,Bao Xiuqin¹²³,Liang Jie¹²³,Du Li¹

Affiliation:

1. Medical Genetics Center, Guangdong Women and Children Hospital, Guangzhou, Guangdong, People’s Republic of China

2. Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, Guangdong, People’s Republic of China

3. Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, Guangdong, People’s Republic of China

Funder

Science and Technology Program of Guangzhou, China

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/16078454.2023.2184118

Reference20 articles.

1. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

2. Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations

3. Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects

4. Hemoglobin variants in southern China: results obtained during the measurement of glycated hemoglobin in a large population

5. Long-Molecule Sequencing

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1. Identification of double heterozygous -α ^4.2Ⅰ /-α ^4.2Ⅱ using third-generation sequencing;Hematology;2023-08-24

2. Third generation sequencing transforms the way of the screening and diagnosis of thalassemia: a mini-review;Frontiers in Pediatrics;2023-07-06