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Hemoglobin
international journal for hemoglobin research
Volume 13, 1989 - Issue 1
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Original Article

A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns

Y. J. Fei Department of Cell, Molecular Biology Medical College of Georgia Augusta, GA, 30912-2100, USA
,
F. Kutlar Department of Cell, Molecular Biology Medical College of Georgia Augusta, GA, 30912-2100, USA
,
H. F. Harris Department of Cell, Molecular Biology Medical College of Georgia Augusta, GA, 30912-2100, USA
,
M. M. Wilson Department of Cell, Molecular Biology Medical College of Georgia Augusta, GA, 30912-2100, USA
,
A. Milana Dipartimento di Pediatrica Cattedra di Ematologia Pediatrica Universita di Catania, 95125, Catania, Italy
,
P. Sciacca Dipartimento di Pediatrica Cattedra di Ematologia Pediatrica Universita di Catania, 95125, Catania, Italy
,
G. Schiliro Dipartimento di Pediatrica Cattedra di Ematologia Pediatrica Universita di Catania, 95125, Catania, Italy
,
B. Masaia Istituto di Fisiologia Generale e Chimica Biologica Universita degli Studi di Sassari, 07100, Sassari, Italy
,
L. Manca Istituto di Fisiologia Generale e Chimica Biologica Universita degli Studi di Sassari, 07100, Sassari, Italy
,
Ç Altay Department of Pediatrics, Children's Medical Center Hacettepe University, Ankara, Turkey
,
A. Gurgey Department of Pediatrics, Children's Medical Center Hacettepe University, Ankara, Turkey
,
J. Ma. de Pablos Servicio de Hematologia, Ciudad Sanitaria “Virgen de las Nieves”, 18014, Granada, Spain
,
A. Villegas Servicio de Hematologia, Universidad Complutense de Madrid Hospital Clinico de San Carlos, 28040, Madrid, Spain
&
T. H. J. Huisman Department of Cell, Molecular Biology Medical College of Georgia Augusta, GA, 30912-2100, USA
 show all
Pages 45-65 | Received 22 Mar 1988, Accepted 11 Aug 1988, Published online: 07 Jul 2009

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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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C. Öner, A. Gürgey, R. Öner, H. Balkan, F. Gümrük, E. Baysal & Ç. Altay. (1997) The Molecular Basis of HB H Disease in Turkey. Hemoglobin 21:1, pages 41-51.
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T. P. Molchanova & T. H. J. Huisman. (1996) The Importance of the 3′ Untranslated Region for the Expression of the α-Globin Genes. Hemoglobin 20:1, pages 41-54.
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M. J. Peres, L. Romão, H. Carreiro, I. Picanço, L. Batalha, H. A. Magalhães, M. C. Martins & J. Lavinha. (1995) Molecular Basis of A-Thalassa in Portugal. Hemoglobin 19:6, pages 343-352.
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RobertT. Jackson. (1993) Hemoglobin comparisons in a sample of European and African American children. Ecology of Food and Nutrition 29:2, pages 139-146.
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A. Villegas, J. Sanchez & E. Sal del Rio. (1992) α-Globin Genotypes in a Spanish Population. Hemoglobin 16:5, pages 427-429.
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Bruno Masala. (1992) Hemoglobinopathies in Sardinia. Hemoglobin 16:4, pages 331-351.
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T. H. J. Huisman, F. Kutlar & L-H. Gu. (1991) γ Chain Abnormalities and γ-Globin Gene Rearrangements in Newborn Babies of Various Populations. Hemoglobin 15:5, pages 349-379.
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D. Plaseska, F. Kutlar, J. B. Wilson, Y. J. Fei & T. H. J. Huisman. (1990) Hb F-Charlotte, an Aγ Variant with a Threonine Residue in Position γ75 and a Glycine Residue in Position γ136. Hemoglobin 14:6, pages 617-625.
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L. Manca & B. Masaia. (1990) A Simple Approach To the Determination of the γ Chain Composition of F in Adult Human Blood Samples. Hemoglobin 14:5, pages 517-527.
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J. M. Gonzalez-Redondo, F. Gilsanz & P. Ricard. (1989) Characterization of a New α-Thalassemia-1 Deletion in a Spanish Family. Hemoglobin 13:2, pages 103-116.
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Nasir Al-Allawi, Sarah Al Allawi & Sana D. Jalal. (2020) Genetic epidemiology of hemoglobinopathies among Iraqi Kurds. Journal of Community Genetics 12:1, pages 5-14.
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Zhenning He, Decheng Song, Sebastiaan van Zalen & J Eric Russell. (2014) Structural determinants of human ζ-globin mRNA stability. Journal of Hematology & Oncology 7:1.
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Wanjun Zhou, Ge Wang, Xuefeng Zhao, Fu Xiong, Shaoxiong Zhou, Jianming Peng, Youming Cheng, Shun Xu & Xiangmin Xu. (2013) A Multiplex qPCR Gene Dosage Assay for Rapid Genotyping and Large-Scale Population Screening for Deletional α-Thalassemia. The Journal of Molecular Diagnostics 15:5, pages 642-651.
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Julio Da Luz, Amalia Ávila, Sandra Icasuriaga, María Gongóra, Luis Castillo, Alejandra Serrón, Elza Miyuki Kimura, Fernando Ferreira Costa, Mónica Sans & Maria de Fátima Sonati. (2013) Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population. Genetics and Molecular Biology 36:3, pages 316-322.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
H. Siala, F. Ouali, T. Messaoud, A. Bibi & S. Fattoum. (2008) α-Thalassaemia in Tunisia: some epidemiological and molecular data. Journal of Genetics 87:3, pages 229-234.
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M. J. Rugless, C. A. Fisher, J. M. Old, J. Sloane-Stanley, H. Ayyub, D. R. Higgs & D. Garrick. (2008) A large deletion in the human  -globin cluster caused by a replication error is associated with an unexpectedly mild phenotype. Human Molecular Genetics 17:19, pages 3084-3093.
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Laura Manca & Bruno Masala. (2008) Disorders of the synthesis of human fetal hemoglobin. IUBMB Life 60:2, pages 94-111.
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HF Pan, GF Long, Q Li, YN Feng, ZY Lei, HW Wei, YY Huang, JH Huang, N Lin, QQ Xu, SY Ling, XJ Chen & T Huang. (2007) Current status of thalassemia in minority populations in Guangxi, China. Clinical Genetics 71:5, pages 419-426.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Akueté Yvon Segbena, Claude Prehu, Henri Wajcman, Josiane Bardakdjian-Michau, Kodjovi Messie, Lochina Feteke, Anne Vovor, Mireille David, Josué Feingold & Frédéric Galacteros. (1998) Hemoglobins in Togolese Newborns: Hb S, Hb C, Hb Bart's, and α-Globin Gene Status. American Journal of Hematology 59:3, pages 208-213.
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Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1998) 1 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 11:1, pages 1-51.
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Gino Schilirò, Elena Mirabile, Rosario Testa, Giovanna Russo-Mancuso & Salvatore P. Dibenedetto. (1997) Presence of hemoglobinopathies in Sicily: A historic perspective. American Journal of Medical Genetics 69:2, pages 200-206.
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Elena Mirabile, Rosario Testa, Piera Samperi, Carmela Consalvo & Vincenzo Romano. (2009) A mild form of Hb S‐β‐thalassemia syndrome is assured in Sicilian patients by β+mutant IVS‐I nt 6(T→C). European Journal of Haematology 58:1, pages 67-69.
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Robert J. Adams, Abdullah Kutlar, Virgil McKie, Elizabeth Carl, Fenwick T. Nichols, Jin Cal Liu, Kathleen McKie & Anthony Clary. (2006) Alpha thalassemia and stroke risk in sickle cell anemia. American Journal of Hematology 45:4, pages 279-282.
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Bruno Masala & Laura Manca. 1994. Hemoglobins Part B: Biochemical and Analytical Methods. Hemoglobins Part B: Biochemical and Analytical Methods 21 44 .
G. Schiliro'P. Samperi, R. Testa, R. B. Gupta, L.‐H. Gu & T. H. J. Huisman. (2006) Clinical, hematological, and molecular features in sicilians with Hb S‐β‐thalassemia. American Journal of Hematology 41:4, pages 264-269.
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Karel Indrak, Vaclav Brabec, Jarmila Indrakova, Ladislav Chrobak, Adriana Sakalova, Marie Jarosova, Jaroslav Cermak, You-jun Fei, Ferdane Kutlar, Yuan-chao Gu, Erol Baysal & Titus H. J. Huisman. (1992) Molecular characterization of β-thalassemia in Czechoslovakia. Human Genetics 88:4, pages 399-404.
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Adrian V.S. Hill. (1992) Molecular epidemiology of the thalassaemias (including haemoglobin E). Baillière's Clinical Haematology 5:1, pages 209-238.
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Robert T. Jackson. (2005) Hemoglobin comparisons between African American and European American males with hemoglobin values in the normal range. American Journal of Human Biology 4:3, pages 313-318.
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Ferdane Kutlar, Hugo Moscoso, Charles R. Kiefer, Frederick A. Garver, Sinan Beksaç, Lütfi Önderoglu, Aytemiz Gurgey, Çigdem Altay & Titus H.J. Huisman. (1991) Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses. Journal of Chromatography B: Biomedical Sciences and Applications 567:2, pages 359-368.
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K. Indrak, Y. J. Fei, H. W. Li, E. Baysal, V. Brabec, H. Fortova, J. Cermak & T. H. J. Huisman. (1991) A Czechoslovakian teenager with Hb E-β∘-thalassemia [IVS-I-1 (G → A)] complicated by the presence of an α-globin gene triplication. Annals of Hematology 63:1, pages 42-44.
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Bruno Masala & Laura Manca. (1991) Detection of the common Hb F Sardinia [Aγ(E19)Ile → Thr]variant by isoelectric focusing in normal newborns and in adults affected by elevated fetal hemoglobin syndromes. Clinica Chimica Acta 198:3, pages 195-202.
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R. Vestri, E. Pieragostini, F. Yang, P. di Gregorio, A. Rando & P. Masina. (2008) Expression of triplicated and quadruplicated α globin genes in sheep. British Journal of Haematology 77:1, pages 110-116.
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Bruno Masala & Laura Manca. (1990) High-performance liquid chromatography of globin chains in the identification of human globin gene abnormalities.. Biophysical Chemistry 37:1-3, pages 225-230.
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A. Villegas, F. Calero, M. A. Vickers, H. Ayyub & D. R. Higgs. (2009) α Thalassaemia in two Spanish families. European Journal of Haematology 44:2, pages 110-115.
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G. Schilirò, M. Spena, E. Giambelluca & A. Maggio. (2006) Sickle hemoglobinopathies in sicily. American Journal of Hematology 33:2, pages 81-85.
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