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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 2
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Original

Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening

Barry Eng Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada
,
Lynda Walker Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada
,
Lisa M. Nakamura Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada
,
Carolyn Hoppe Children's Hospital and Research Center at Oakland, Oakland, California, USA
,
Mahin Azimi Children's Hospital and Research Center at Oakland, Oakland, California, USA
,
Helen Lee Children's Hospital and Research Center at Oakland, Oakland, California, USA
&
John S. Waye Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, CanadaCorrespondence[email protected]
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Pages 129-134 | Received 07 Jul 2006, Accepted 19 Oct 2006, Published online: 07 Jul 2009

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Zeyong Li, Lei Li, Yachao Yao, Nan Li, Yahong Li, Zhen Zhang, Fang Yan, Houkuang Qiu, Chunyan Wu & Zhi Zhang. (2015) A Novel Promoter Mutation (HBB: c.-75G>T) Was Identified as a Cause of β+-Thalassemia. Hemoglobin 39:2, pages 115-120.
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John S. Waye, Lisa M. Nakamura-Garrett, Barry Eng, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2011) β+-Thalassemia Trait Due to a Novel Mutation in the β-Globin Gene Promoter: −26 (A>C) [HBB c.−76A>C]. Hemoglobin 35:1, pages 84-86.
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Articles from other publishers (9)

Maria Jackson & Daniel Stobo. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences 1 12 .
Jiwu Lou, Yuhua Ye, Manna Sun, Ying Zhao, Youqing Fu & Yanhui Liu. (2022) A stepwise haematological screening and whole‐exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A 2 from a cohort of 47336 individuals . International Journal of Laboratory Hematology 45:1, pages 90-95.
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Lourdes del Carmen Rizo-de la TorreVíctor Manuel Rentería-LópezJosefina Yoaly Sánchez-LópezMaría Teresa Magaña-TorresBertha Ibarra-CortésFrancisco Javier Perea-Díaz. (2021) Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients. Genetic Testing and Molecular Biomarkers 25:3, pages 247-252.
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Mikhail Ponomarenko, Ekaterina Sharypova, Irina Drachkova, Irina Chadaeva, Olga Arkova, Olga Podkolodnaya, Petr Ponomarenko, Nikolay Kolchanov & Ludmila Savinkova. (2020) Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders. BMC Medical Genetics 21:S1.
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Jing Zeng, Yuxuan Wu, Chunyan Ren, Jasmine Bonanno, Anne H. Shen, Devlin Shea, Jason M. Gehrke, Kendell Clement, Kevin Luk, Qiuming Yao, Rachel Kim, Scot A. Wolfe, John P. Manis, Luca Pinello, J. Keith Joung & Daniel E. Bauer. (2020) Therapeutic base editing of human hematopoietic stem cells. Nature Medicine 26:4, pages 535-541.
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Jason M Gehrke, Oliver Cervantes, M Kendell Clement, Yuxuan Wu, Jing Zeng, Daniel E Bauer, Luca Pinello & J Keith Joung. (2018) An APOBEC3A-Cas9 base editor with minimized bystander and off-target activities. Nature Biotechnology 36:10, pages 977-982.
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Gabriella E. Martyn, Kate G.R. Quinlan & Merlin Crossley. (2017) The regulation of human globin promoters by CCAAT box elements and the recruitment of NF-Y. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms 1860:5, pages 525-536.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSwee Lay Thein & William G. Wood. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 323 356 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 321 322 .

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