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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 4
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Original Article

Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain

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Pages 369-377 | Received 13 Sep 2012, Accepted 22 Dec 2012, Published online: 15 Apr 2013

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (2)

Milad Rafat, Zeinab Allamehzadeh, Mohammad Shekari, Masoumeh Afsa & Kianoosh Malekzadeh. (2021) The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study. Hemoglobin 45:4, pages 234-238.
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Articles from other publishers (4)

Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Stacy Colaco, Roshan Colah & Anita Nadkarni. (2022) Significance of borderline HbA2 levels in β thalassemia carrier screening. Scientific Reports 12:1.
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Stacy Colaco & Anita Nadkarni. (2021) Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers. Mutation Research/Reviews in Mutation Research 788, pages 108387.
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Lucia Dora Notarangelo, Annalisa Agostini, Maddalena Casale, Piera Samperi, Francesco Arcioni, Paolo Gorello, Silverio Perrotta, Nicoletta Masera, Angelica Barone, Elisa Bertoni, Elisa Bonetti, Roberta Burnelli, Tommaso Casini, Giovanni Carlo Del Vecchio, Beatrice Filippini, Fiorina Giona, Paola Giordano, Chiara Gorio, Eleonora Marchina, Margherita Nardi, Angela Petrone, Raffaella Colombatti, Laura Sainati & Giovanna Russo. (2019) HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype‐phenotype correlation. European Journal of Haematology 104:3, pages 214-222.
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