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Hemoglobin
international journal for hemoglobin research
Volume 35, 2011 - Issue 4
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Original Article

Sickle Cell/β0-Thalassemia Associated With the 1393 bp Deletion Can be Associated With a Severe Phenotype

Yvonne DanielBlood Sciences, Guy’s and St. Thomas’ Pathology, St. Thomas’ Hospital, London, UK
,
Kim HillBlood Sciences, Guy’s and St. Thomas’ Pathology, St. Thomas’ Hospital, London, UK
,
Baba InusaDepartment of Paediatrics, Evelina Hospital, Guy’s and St. Thomas’ National Health Service Foundation Trust, London, UK
,
Swee Lay TheinKing’s College London School of Medicine, Division of Gene and Cell Based Therapy, King’s Denmark Hill Campus, London, UK;King’s College Hospital National Health Service Foundation Trust, Department of Haematological Medicine, Denmark Hill, London, UK
&
Jo HowardDepartment of Haematology, Guy’s and St. Thomas’ National Health Service Foundation Trust, London, UKCorrespondence[email protected]
Pages 406-410 | Received 02 Mar 2011, Accepted 11 Apr 2011, Published online: 28 Jul 2011

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Read on this site (3)

John S. Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker & Barry Eng. (2017) Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene. Hemoglobin 41:4-6, pages 239-242.
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Bruno Deltreggia Benites, Stephany Oliveira Bastos, Gabriel Baldanzi, Allan de Oliveira dos Santos, Celso Dario Ramos, Fernando Ferreira Costa, Simone Cristina Olenscki Gilli & Sara Teresinha Olalla Saad. (2016) Sickle cell/β-thalassemia: Comparison of Sβ0 and Sβ+ Brazilian patients followed at a single institution. Hematology 21:10, pages 623-629.
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Sakorn Pornprasert, Sitthichai Panyasai, Kanyakan Kongthai & Kallayanee Treesuwan. (2012) Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-Thalassemia Codon 17 (A>T) in a Thai Patient. Hemoglobin 36:3, pages 265-269.
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Articles from other publishers (1)

Bruno Deltreggia Benites, Ianara Silva Cisneiros, Stephany Oliveira Bastos, Ana Paula Beppler Lazaro Lino, Fernando Ferreira Costa, Simone Cristina Olenscki Gilli & Sara Teresinha Olalla Saad. (2019) Echocardiografic abnormalities in patients with sickle cell/β-thalassemia do not depend on the β-thalassemia phenotype. Hematology, Transfusion and Cell Therapy 41:2, pages 158-163.
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