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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 5
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Short Communication

A novel 6.3 kb deletion and the Rare 27.6 kb Deletion Causing α+-Thalassemia in two Chinese Patients

Xian-Yao WangDepartment of Pediatrics, Shantou Central Hospital, Affiliated to Shantou Hospital of Sun Yat-Sen University, Shantou, People’s Republic of China;
,
Ming-Xiang LinDepartment of Pediatrics, Shantou Central Hospital, Affiliated to Shantou Hospital of Sun Yat-Sen University, Shantou, People’s Republic of China;
&
Min LinDepartment of Histology and Embryology, Shantou University Medical College, Shantou, People’s Republic of ChinaCorrespondence[email protected]
Pages 365-368 | Received 07 Apr 2016, Accepted 24 Jun 2016, Published online: 22 Sep 2016

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Ke Wang, Ting Yi, Wen-Tao Wu, Juan Lu, Li-Na He, Hong-Ping Zhou, Jiang-Wei Ke & Fa-Di Liu. (2022) Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People’s Republic of China. Hemoglobin 46:5, pages 272-276.
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Articles from other publishers (2)

Aubrey Milunsky & Jeff M. MilunskyJohn M. Old & Jan Traeger‐Synodinos. 2021. Genetic Disorders and the Fetus. Genetic Disorders and the Fetus 1002 1034 .
Gülüzar Özbolat & Abdullah Tuli. (2017) Talasemi ve ilgili hemoglobinopatilerin Moleküler Tanı Yöntemleri: Günümüz ve GelecekMolecular Diagnostics Methods of Thalassemia and related hemoglobinopathies: Present and Future. Adıyaman Üniversitesi Sağlık Bilimleri Dergisi 3:3, pages 599-616.
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