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Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 4
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Original Article

HB Watts [α74(EF3) OR α75(EF4)ASP→0]: A Shortened α Chain Variant Due to the Deletion of Three Nucleotides in Exon 2 of the α2-Globin Gene

S. Rahbar Hemoglobin Research Laboratory City of Hope National Medical Center, Duarte, CA, 91010-0269, USA
,
C. Lee Western Women's Medical Clinic, Los Angeles, CA, 90062, USA
,
V. F. Fairbanks Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA
,
D. J. McCormick Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA
,
K. Kubik Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA
,
B. J. Madden Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA
&
G. Nozari Hemoglobin Research Laboratory City of Hope National Medical Center, Duarte, CA, 91010-0269, USA
 show all
Pages 321-330 | Received 15 Jul 1996, Accepted 03 Mar 1997, Published online: 07 Jul 2009

Citations (11)

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Henri Wajcman, Alexandre G. de Brevern, Jean Riou, Celine Latouche, Michael C. Marden & Serge Pissard. (2018) Short in-Frame Insertions/Deletions in the Coding Sequence of the α-Globin Gene. Consequences of the 3D Structure and Resulting Phenotypes: Hb Choisy as an Example. Hemoglobin 42:5-6, pages 287-293.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Laurie A. Steiner, Jack Van Hoff, Ferdane Kutlar & Patrick G. Gallagher. (2007) Aplastic Crisis Revealing the Diagnosis of Hb Evans [α62(E11)Val→Met, GTG→ATG (α2)] in a Hispanic Kindred: Case Report and Review. Hemoglobin 31:4, pages 409-416.
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Nelly Burnichon, Philippe Lacan, Michel Becchi, Isabelle Zanella-Cleon, Martine Aubry, Mohammed Mowafy, Nicole Couprie & Alain Francina. (2006) A New α Chain Hemoglobin Variant: Hb Al-Hammadi Riyadh [α75(EF4)Asp→Val (α2)]. Hemoglobin 30:2, pages 155-164.
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T. H.J. Huisman & M. F.H. Carver. (1998) The Thalassemia Repository (Ninth Edition; Part II). Hemoglobin 22:3, pages 287-310.
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J. Hitchen, A. McFarlane, J. Lafferty & M. A.M. Ali. (1998) Detection of α2- and α1- Globin Gene Variants by a Modified Cycle Sequencing Method. Hemoglobin 22:4, pages 373-376.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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Articles from other publishers (4)

Maria Luisa González Borrachero, Félix de la Fuente-Gonzalo, Fernando Ataúlfo González, Jorge M. Nieto, Ana Villegas & Paloma Ropero. (2015) Delta0-talasemia por inserción de 27 pares de bases en el gen δ-globina con descenso de los valores de hemoglobina A2. Medicina Clínica 144:7, pages 312-316.
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Maria Luisa González Borrachero, Félix de la Fuente-Gonzalo, Fernando Ataúlfo González, Jorge M. Nieto, Ana Villegas & Paloma Ropero. (2015) Delta0-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A2 levels. Medicina Clínica (English Edition) 144:7, pages 312-316.
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Joanne Traeger-Synodinos, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Christina Vrettou, Alexandra Stamoulakatou & Emmanuel Kanavakis. (2000) Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies. Blood Cells, Molecules, and Diseases 26:4, pages 276-284.
Crossref
Luigi F. Bernini & Cornelis L. Harteveld. (1998) 2 α-Thalassaemia. Baillière's Clinical Haematology 11:1, pages 53-90.
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