Identification of a Novel 9.7 kb Deletion Causing α0-Thalassemia in Two Pregnant Women in Southern China-Reference-Cited by-同舟云学术

Identification of a Novel 9.7 kb Deletion Causing α0-Thalassemia in Two Pregnant Women in Southern China

Published:2018-05-04 Issue:3 Volume:42 Page:209-212
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Lin Li¹,Yang Qi¹,Zhang Shujie¹,Zuo Yangjng¹,He Sheng¹,Xu Xiangmin¹,Chen Biyan¹^ORCID,Qiu Xiaoxia¹

Affiliation:

1. Laboratory of Genetics and Metabolism, Guangxi Zhuang Autonomous Region Women and Children Care Hospital, Xiangzhu, Nanning, Guangxi Zhuang Autonomous Region, People’s Republic of China

Funder

Natural Science Foundation of China

Natural Science Foundation of Guangxi

Health Department of Guangxi Province

Guangxi Science and Technology Project

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1516673

Reference9 articles.

1. Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

2. The α-Thalassemias

3. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH

4. Identification of a novel 44.6-kb deletion causing α0 -thalassemia in southern China

5. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening

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