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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 1
49
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Short Communication

A New High A2‐β‐Thalassemia Due to a 468 bp Deletion (− 475 to − 8) in the β‐Globin Gene Promoter of the Intact β‐Globin Structural Gene

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Pages 69-72 | Received 29 Aug 2003, Accepted 05 Sep 2003, Published online: 24 Aug 2009

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Read on this site (2)

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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Margie Patterson, Lynda Walker, Barry Eng & John S. Waye. (2005) High Hb A2 β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia. Hemoglobin 29:4, pages 293-295.
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Articles from other publishers (3)

Serge Pissard, Valérie Raclin, Philippe Lacan, Caroline Garcia, Patricia Aguilar-Martinez, Alain Francina & Philippe Joly. (2013) Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas. Clinica Chimica Acta 415, pages 35-40.
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Philippe Joly, Philippe Lacan, Caroline Garcia, Nicole Couprie & Alain Francina. (2009) Identification and molecular characterization of four new large deletions in the β-globin gene cluster. Blood Cells, Molecules, and Diseases 43:1, pages 53-57.
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Rosalba Di Marzo, Santina Acuto, Roberta Calzolari & Aurelio Maggio. (2005) Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and δβ° thalassemia patients. Experimental Hematology 33:11, pages 1363-1370.
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