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Hemoglobin
international journal for hemoglobin research
Volume 2, 1978 - Issue 6
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Original Article

δβ-Thalassemia in a Mexican Family: Clinical Differences Among Homozygotes

Guillermo Ruiz Reyes Laboratories Clinicos de Puebla, Hospital del Issste, Puebla, Pue, Mexico
,
Arturo Piña-Camara Hospital del Issste, Tuxtla, Gutiérrez, Chis, Mexico
,
A. E. Felice Departments of Cell and Molecular Biology, Medicine Medical College of Georgia and Veterans Administration Hospital, Augusta, GA, 30901, USA
,
M. E. Gravely Departments of Cell and Molecular Biology, Medicine Medical College of Georgia and Veterans Administration Hospital, Augusta, GA, 30901, USA
&
T. H. J. Huisman Departments of Cell and Molecular Biology, Medicine Medical College of Georgia and Veterans Administration Hospital, Augusta, GA, 30901, USA
Pages 513-529 | Received 06 Oct 1978, Accepted 27 Nov 1978, Published online: 07 Jul 2009

Citations (11)

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Read on this site (5)

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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Guillermo Ruiz Reyes. (1983) Hemoglobin Variants in Mexico. Hemoglobin 7:6, pages 603-610.
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G. Dincol, C. Altay, M. Aksoy, A. Gurgey, A. E. Felice & T. H. J. Huisman. (1981) Clinical and Hematological Evaluation of two δ0 δ0 - Thalassemia Homozygotes. Hemoglobin 5:2, pages 153-164.
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. (1981) The First Homozygote for the Hereditary Persistence of Fetal Hemoglobin Observed in the Southeastern United States. Hemoglobin 5:4, pages 411-416.
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L. B. Wilson, T. H. J. Huisman & J. T. Wilson. (1980) Gene Structure in Hereditary Persistence of Fetal Hemoglobin Individuals. Hemoglobin 4:3-4, pages 509-518.
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Articles from other publishers (6)

Li Du, Danqing Qin, Jicheng Wang, Lihua Yu, Cuize Yao, Ling Liu, Yanxia Zhang, Tingting Hu, Tenglong Yuan, Jie Liang & Aihua Yin. (2020) Genetic and phenotypic analysis of a rare asymptomatic case of a homozygous Chinese Gγ+(Aγδβ)0-thalassemia deletion in a Chinese family. Clinical Biochemistry 76, pages 11-16.
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Patricia A. OnealNicole M. GanttJoseph D. SchwartzNatarajan V. BhanuY. Terry LeeJohn W. MoroneyChristopher H. ReedAlan N. SchechterNaomi L. C. LubanJeffery L. Miller. (2006) Fetal hemoglobin silencing in humans. Blood 108:6, pages 2081-2086.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
GINO SCHILIRÓ, SALVATORE MUSUMECI, MARIA ANTONIETTA ROMEO, FELICIA GREGORIO, ALFONSINA D'AGATA, ROSARIO TESTA & GIUSEPPE RUSSO. (1985) Clinical and Molecular Heterogeneity of ?, ?-Thalassemia in Sicily. Annals of the New York Academy of Sciences 445:1 Fifth Cooley', pages 148-158.
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A. B. Amin, N. L. Pandya, P. P. Diwin, P. D. Darbre, C. Kattamis, A. Metaxatou‐Mavromati, J. M. White, W. G. Wood, J. B. Clegg & D. J. Weatherall. (2008) A Comparison of the Homozygous States for G γ and G γ A γδβ Thalassaemia . British Journal of Haematology 43:4, pages 537-548.
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W. G. Wood, J. B. Clegg & D. J. Weatherall. (2008) HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (HPFH) AND δβ THALASSAEMIA. British Journal of Haematology 43:4, pages 509-520.
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