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Blood|February 2, 2019
Editing aberrant splice sites efficiently restores β-globin expression in β-thalassemiaShuqian Xu, Kevin Luk, Qiuming Yao, et al.
Stem Cells (Dayton, Ohio)|August 5, 2006
Sequential analysis of alpha- and beta-globin gene expression during erythropoietic differentiation from primate embryonic stem cellsKatsutsugu Umeda, Toshio Heike, Mami Nakata-Hizume, et al.
Molecular and Cellular Biology|April 30, 2008
A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin FZhiyi Chen, Hong-Yuan Luo, Raveen K Basran, et al.
Hemoglobin|April 12, 2017
Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan FamilyAllan Pernudy-Ubau, Jaslyn Salinas-Molina, Yaneris Requenez, et al.
Hemoglobin|October 28, 2014
Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemiaHeather L Edward, Louis Almero Du Pisani, Walter E Rodriguez-Romero, et al.
American Journal of Hematology|August 4, 2009
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patientsSara C Koenig, Esmira Becirevic, Miriam S C Hellberg, et al.
Stem Cell Reports|January 24, 2017
A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem CellsSeonmi Park, Andreia Gianotti-Sommer, Francisco Javier Molina-Estevez, et al.
Blood Cells, Molecules & Diseases|March 8, 2013
Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotypeDuyen Ngo, Harold Bae, Martin H Steinberg, et al.
British Journal of Haematology|January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotesZhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
Blood|March 10, 2011
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionJohn J Farrell, Richard M Sherva, Zhi-Yi Chen, et al.
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