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Hemoglobin
international journal for hemoglobin research
Volume 15, 1991 - Issue 5
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Original Article

γ Chain Abnormalities and γ-Globin Gene Rearrangements in Newborn Babies of Various Populations

T. H. J. Huisman Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
F. Kutlar Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
L-H. Gu Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 349-379 | Received 06 Mar 1991, Accepted 10 Jul 1991, Published online: 07 Jul 2009

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Ho-Wan Ip & Chi-Chiu So. (2013) Diagnosis and prevention of thalassemia. Critical Reviews in Clinical Laboratory Sciences 50:6, pages 125-141.
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Chien-Hao Huang, Yih-Yuan Chang, Chung-Hsiung Chen & Tsang-Ming Ko. (2008) Molecular Characterization of a β-Globin Gene Deletion of 1357 bp in a Taiwanese β-Thalassemia Carrier. Hemoglobin 32:5, pages 498-504.
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Svetlana Pulis, Christian A. Scerri, Pierre Schembri Wismayer, Ruth Galdies, Stephanie Bezzina Wettinger & Alex E. Felice. (2007) Developmental Effect of the XmnI Site on Gγ-Globin Gene Expression Among Newborn Hb F-Malta-I [Gγ117(G19)His→Arg, CAT→CGT] Heterozygotes and Adult β+-Thalassemia Homozygotes. Hemoglobin 31:1, pages 71-82.
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Monica Pirastru, Laura Manca, Marcella Palici di Suni, Silvia Maria Speziga & Bruno Masala. (2004) Hb F‐Porto Torres [Aγ75(E19)Ile→Thr, 136(H14)Ala→Ser]: A Novel Variant of the Aγ Chain Having Two Substitutions, One Being that of Hb F‐Sardinia. Hemoglobin 28:4, pages 297-303.
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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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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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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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G. D. Efremov, A. J. Dimovski, Z. Popovski, S. Janeva, D. Plaseska, L. Simjanovska, E. Sukarova, A. Momirovska, M. Lazarevski & R. Kuljan. (1996) The γ-Globin Gene Rearrangements in Newborns from the Repuc of Macedonia. Hemoglobin 20:4, pages 401-414.
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M. A. Çürük, S. C. Howard, A. Kutlar & T. H. J. Huisman. (1995) A Newly Discovered β°-Thalassemia (IVS-11-850, G→A) Mutation in a North European Family. Hemoglobin 19:3-4, pages 207-211.
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L-H. Gu, C. Öner & T. H.J. Huisman. (1995) The GγT Chain (Gγ75 Thr; 136 Gly) In Hb F-Charlotte Is The Product Of An Aγ Gene With A Limited Gene Conversion And That In Hb F-Waynesboro Of A Mutated Gγ Gene. Hemoglobin 19:6, pages 413-418.
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J. M. de Pablos Gallego, L-H. Gu, J. Ye. Leonova & T. H.J. Huisman. (1995) Hb F-Vea or α2Gγ240(C6)Arg→Gly. Hemoglobin 19:6, pages 407-411.
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W-D. Chen, P-C. Jia, S-S. Chen, C-C. Liang, B-S. Wang, S. Gao, X-J. Wang, M. Wang & S-K. Qu. (1994) The Gγ:Aγ ratios in the fetal hemoglobin of newborns of the man ethnic group and their γ-globin gene arrangements. Hemoglobin 18:3, pages 193-199.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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P. Ferranti, F. Barone, P. Pucci, A. Malorni, G. Marino, G. Pilo, L. Manca & B. Masaia. (1994) Hb F-Sassari: A Novel Gγ Variant with a Threonine Residue at Position γ75, Characterized by Mass Spectrometry Techniques. Hemoglobin 18:4-5, pages 307-315.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
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T. P. Molchanova, J. B. Wilson, L-H. Gu, R. D. W. Hain, L. S. Chang, A. O. Poon & T. H. J. Huisman. (1992) A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α2Gγ292(F8)HIS→TYR. Hemoglobin 16:5, pages 389-398.
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Articles from other publishers (13)

Jean-Yves Métais, Phillip A. Doerfler, Thiyagaraj MayuranathanDaniel E. Bauer, Stephanie C. FowlerMatthew M. Hsieh, Varun KattaSagar KeriwalaCicera R. LazzarottoKevin Luk, Michael D. NeelS. Scott PerrySamuel T. Peters, Shaina N. Porter, Byoung Y. RyuAkshay Sharma, Devlin SheaJohn F. TisdaleNaoya UchidaScot A. Wolfe, Kaitly J. WoodardYuxuan WuYu YaoJing ZengShondra Pruett-Miller, Shengdar Q. Tsai & Mitchell J. Weiss. (2019) Genome editing of HBG1 and HBG2 to induce fetal hemoglobin. Blood Advances 3:21, pages 3379-3392.
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Harry Bard, Ann M. English, Karine Bellemin & Carmen Gagnon. (2004) Developmental changes in NO bioavailability in fetal erythrocytes. Seminars in Perinatology 28:4, pages 312-316.
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R. Hojas, A. Villegas, P. Ropero, F. Valverde, A. Nogales, F. A. González, C. José, L. Villar & C. García. (2003) Two new mutations in cis on Gγ chain of fetal hemoglobin: Hb F-Madrid [Gγ50(D1)Ser→Cys] and [Gγ75(E19)Ile→Thr]. Annals of Hematology 82:3, pages 181-183.
Crossref
Isabel Gonçalves, João Lavinha, Rolande Ducrocq & Leonor Osório-Almeida. (2002) A novel rearrangement of the human fetal globin genes leading to a six γ-globin gene haplotype. British Journal of Haematology 116:2, pages 454-457.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
T.H.J. Huisman. (1997) Gamma chain abnormal human fetal hemoglobin variants. American Journal of Hematology 55:3, pages 159-163.
Crossref
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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Julia Ye. Leonova, Elena G. Kazanetz, Natalia S. Smetanina, Adekunle D. Adekile, Georgi D. Efremov & Titus H.J. Huisman. (1996) Variability in the fetal hemoglobin level of the normal adult. American Journal of Hematology 53:2, pages 59-65.
Crossref
Mudra Kohli‐Kumar, Theodore Zwerdling & Donald L. Rucknagel. (2006) Hemoglobin F‐Cincinnati, α 2 G γ 2 41(C7) Phe → Ser in a newborn with cyanosis . American Journal of Hematology 49:1, pages 43-47.
Crossref
M. B. Coleman, J. G. AdamsIIIIII, M. H. Steinberg & W. P. Winter. (2006) A four base pair deletion 5′ to the A γ T gene is associated not only with decreased expression of the A γ T ‐globin gene, but also of the G γ‐globin gene in cis . American Journal of Hematology 47:4, pages 307-311.
Crossref
A. J. Dimovski, A. D. Adekile & T. H. J. Huisman. (1994) The in vivo expression of the globin genes of theβ cistron in γ-,δ-, andδβ-thalassemia heterozygotes. Experientia 50:2, pages 167-170.
Crossref
Bruno Masala & Laura Manca. 1994. Hemoglobins Part B: Biochemical and Analytical Methods. Hemoglobins Part B: Biochemical and Analytical Methods 21 44 .
Titus H.J. Huisman. (1993) 1 The structure and function of normal and abnormal haemoglobins. Baillière's Clinical Haematology 6:1, pages 1-30.
Crossref

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