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

β-Thalassemia Intermedia in Two Turkish Families is Caused by the Interaction of HB Knossos [β27(B9)ALA→SER] and of HB City of hope [β69(E13)Gly→Ser] with B°-Thalassemia

A. Kutlar Laboratory of Protein Chemistry and Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-1100, USA; Department of Medicine, Hematology Section, Istanbul University Medical School, Çapa Istanbul, Turkey
,
F. Kutlar Laboratory of Protein Chemistry and Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-1100, USA
,
M. Aksoy Department of Medicine, Hematology Section, Istanbul University Medical School, Çapa Istanbul, Turkey
,
A. Gurgey Children's Medical Center Hacettepe University, Ankara, Turkey
,
Ç. Altay Children's Medical Center Hacettepe University, Ankara, Turkey
,
J. B. Wilson Laboratory of Protein Chemistry and Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-1100, USA
,
J. C. Diaz-Chico Laboratory of Protein Chemistry and Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-1100, USA
,
H. Hu Laboratory of Protein Chemistry and Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-1100, USA
&
T. H. J. Huisman Laboratory of Protein Chemistry and Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-1100, USA
 show all
Pages 7-16 | Received 22 Jan 1988, Accepted 26 Jul 1988, Published online: 07 Jul 2009

Citations (16)

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Jian-Ying Zhou, Fan Jiang, Jian Li, Gui-Lan Chen & Dong-Zhi Li. (2019) Coinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization. Hemoglobin 43:2, pages 145-147.
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Ghazi O. Tadmouri & A. Nazlı Başak. (2001) β-THALASSEMIA IN TURKEY: A REVIEW OF THE CLINICAL, EPIDEMIOLOGICAL, MOLECULAR, AND EVOLUTIONARY ASPECTS. Hemoglobin 25:2, pages 227-239.
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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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T. H. J. Huisman. (1993) The β- and δ-Thalassemia Repository (Seventh Edition). Hemoglobin 17:5, pages 479-499.
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M. De Angioletti, G. Maglione, P. Ferranti, C. de Bonis, G. Lacerra, A. Scarallo, L. Pagano, G. Fioretti, R. Cutolo, A. Malorni, P. Pucci & C. Carestia. (1992) HB City of Hope [β69(E13)GLY→SER] in Italy: Association of the Gene with Haplotype IX. Hemoglobin 16:1-2, pages 27-34.
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T. H. J. Huisman. (1992) The β- and δ-Thalassemia Repository. Hemoglobin 16:4, pages 237-258.
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R. Öner, C. Altay, A. Gurgey, M. Aksoy, Y. Kilinc, T. A. Stoming, A. L. Reese, A. Kutlar, F. Kutlar & T. H. J. Huisman. (1990) β-Thalassemia in Turkey. Hemoglobin 14:1, pages 1-13.
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Articles from other publishers (9)

Selahaddin Tekeş, Diclehan Oral, Murat Söker, Selda Şimşek, Veysiye Hülya Uzel & Mehmet Akif Çürük. (2022) Analysis of beta globin gene mutations in Diyarbakir. Turkish Journal of Biochemistry 47:1, pages 113-118.
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Lauren J. Isley, Aleisha K. Chamberlain, Pamela Callum & Jaime Shamonki. (2021) Comparison of methodologies to detect hemoglobinopathy carriers in a multi‐ethnic sperm donor population. Journal of Genetic Counseling 30:5, pages 1399-1406.
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Rosalina Martínez-López, Félix de la Fuente-Gonzalo, Jorge M. Nieto, Cristina Ballesteros Gallar, Carlos Romero Román, Ana Villegas, Fernando A. González, Rafael Martínez, Laura Navarro Casado & Paloma Ropero. (2016) Different forms of Hb Le Lamentin. An unexpected finding in Hba1c quantification. Clinical Biochemistry 49:1-2, pages 57-60.
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Margherita Vinciguerra, Cristina Passarello, Filippo Leto, Filippo Cassarà, Monica Cannata, Aurelio Maggio & Antonino Giambona. (2015) Co-inheritance of the rare β hemoglobin variants Hb Yaounde, Hb Görwihl and Hb City of Hope with other alterations in globin genes: impact in genetic counseling. European Journal of Haematology 94:4, pages 322-329.
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Hengameh Nasouhipur, Ali Banihashemi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki. (2014) Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia. Indian Journal of Hematology and Blood Transfusion 30:S1, pages 243-245.
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Ibrahim KeserEsra ManguogluOzlem KayisliAkif YesilipekGuven Luleci. (2007) Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major. Genetic Testing 11:3, pages 228-230.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
RENZO GALANELLO & ANTONIO CAO. (1998) Relationship between Genotype and Phenotype: Thalassemia Intermediaa. Annals of the New York Academy of Sciences 850:1 COOLEY'S ANEM, pages 325-333.
Crossref
Ç. ALTAY & A. GÜRGEY. (1990) ?-Thalassemia Intermedia in Turkey. Annals of the New York Academy of Sciences 612:1 Sixth Cooley', pages 81-89.
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