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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 5
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Original Article

Molecular Genetic Studies in Black Families with Sickle Cell Anemia and Unusually High Levels of Fetal Hemoglobin

W. K. Seltzer Department of Pediatrics, University of Colorado School Medicine, Denver, CO, 80262, USA; Department of Pediatrics, University of Colorado School Medicine, Denver, CO, 80262, USA
,
T. C. Abshire Department of Pediatrics, University of Colorado School Medicine, Denver, CO, 80262, USA; Department of Biochemistry, Biophysics and Genetics, University of Colorado School Medicine, Denver, CO, 80262, USA
,
P. A. Lane Department of Pediatrics, University of Colorado School Medicine, Denver, CO, 80262, USA; Colorado Sickle Cell Treatment and Research Center University of Colorado School Medicine, Denver, CO, 80262, USA
,
J. S. Roloff Department of Pediatrics, University of Colorado School Medicine, Denver, CO, 80262, USA; Denver Children's Hospital Kempe Research Center, Denver, CO, 80224, USA
&
J. H. Githed Department of Pediatrics, University of Colorado School Medicine, Denver, CO, 80262, USA; Colorado Sickle Cell Treatment and Research Center University of Colorado School Medicine, Denver, CO, 80262, USA
Pages 363-377 | Received 12 Feb 1992, Accepted 01 Jun 1992, Published online: 07 Jul 2009

Citations (11)

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Read on this site (1)

Jialing Cui, Mahin Azimi, Christoph Baysdorfer, Elliott P. Vichinsky & Carolyn C. Hoppe. (2013) Application of Multiplex Ligation-Dependent Probe Amplification to Screen for β-Globin Cluster Deletions: Detection of Two Novel Deletions in a Multi Ethnic Population. Hemoglobin 37:3, pages 241-256.
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Articles from other publishers (10)

Michael Tarasev, Marina Muchnik, Lucia Light, Kenneth Alfano & Sumita Chakraborty. (2017) Individual variability in response to a single sickling event for normal, sickle cell, and sickle trait erythrocytes. Translational Research 181, pages 96-107.
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Suha Mustafa Hassan, Muhanna Al Muslahi, Muna Al Riyami, Abeer Al Balushi, Egbert Bakker, Cornelis L. Harteveld & Piero C. Giordano. (2015) Haplotypes, Sub-Haplotypes and Geographical Distribution in Omani Patients with Sickle Cell Disease. Thalassemia Reports 5:1, pages 4739.
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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 .
Lalitha V. Pillai, Saifuddin Husainy, Sameer Gosavi & Narendra Vaidya. (2005) Sudden unexpected death in an undiagnosed sickle disease. Indian Journal of Critical Care Medicine 9:2, pages 92-95.
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A. Inati, A. Taher, W. Bou Alawi W, S. Koussa, H. Kaspar, H. Shbaklo & P. A. Zalloua. (2003) β-Globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon. European Journal of Haematology 70:2, pages 79-83.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Wendy H. RaskindKathy K. NiakanJohn WolffMark MatsushitaTy VaughanGeorge StamatoyannopoulosChiaki WatanabeJacinda RiosHans D. Ochs. (2000) Mapping of a syndrome of X-linked thrombocytopenia with thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia. Blood 95:7, pages 2262-2268.
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Wendy H. RaskindKathy K. NiakanJohn WolffMark MatsushitaTy VaughanGeorge StamatoyannopoulosChiaki WatanabeJacinda RiosHans D. Ochs. (2000) Mapping of a syndrome of X-linked thrombocytopenia with thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia. Blood 95:7, pages 2262-2268.
Crossref
Kabita Bhaumik. (2006) Fetal hemoglobin synthesis in sickle cell anemia: Some molecular considerations. American Journal of Hematology 46:2, pages 101-106.
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