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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 1
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A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major

Eunice S. EdisonDepartment of Haematology, Christian Medical College, Vellore, India
,
Rajkumar S. VenkatesanDepartment of Haematology, Christian Medical College, Vellore, India
,
Sankari Devi GovindanattarDepartment of Haematology, Christian Medical College, Vellore, India
,
Biju GeorgeDepartment of Haematology, Christian Medical College, Vellore, India
&
Ramachandran V. ShajiDepartment of Haematology, Christian Medical College, Vellore, IndiaCorrespondence[email protected]
Pages 98-102 | Received 23 May 2011, Accepted 28 Jun 2011, Published online: 10 Jan 2012

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Sheng He, Qian Qin, Li Lin, Yangjin Zuo, Qiuli Chen, Honghwei Wei, Chenguang Zheng, Biyan Chen & Xiaoxia Qiu. (2018) First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family. Hemoglobin 42:4, pages 272-275.
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Sheng He, Li Lin, Yuan Wei, Biyan Chen, Shang Yi, Qiuli Chen, XiaoXia Qiu, Hongwei Wei, Guojian Li & Chenguang Zheng. (2016) Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family. Hemoglobin 40:4, pages 277-279.
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Articles from other publishers (2)

Anila Venugopal, Manojkumar Chandran, Nimmisha Eruppakotte, Soumya Kizhakkillach, Sanuj C. Breezevilla & Balachandar Vellingiri. (2018) Monogenic diseases in India. Mutation Research/Reviews in Mutation Research 776, pages 23-31.
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Roshan B. Colah & Ajit Gorakshakar. (2014) Control of Thalassemia in India. Thalassemia Reports 4:2, pages 1955.
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