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Hemoglobin
international journal for hemoglobin research
Volume 5, 1981 - Issue 1
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Original Article

β Thalassemia Associated with Increased HB F Production. Evidence for the Existence of a Heterocellular Hereditary Persistence of Fetal Hemoglobin (Hpfh) Determinant Linked to β Thalassemia in a Southern Italian Population

M. Marinucci Laboratorio di Patologia non Infettiva Istituto Superiore di Sanità, Roma, Italy
,
F. Mavilio Laboratorio di Patologia non Infettiva Istituto Superiore di Sanità, Roma, Italy
,
A. Giuliani Laboratorio di Patologia non Infettiva Istituto Superiore di Sanità, Roma, Italy
,
M. Gabbianelli Laboratorio di Patologia non Infettiva Istituto Superiore di Sanità, Roma, Italy
,
L. Tentori Laboratorio di Patologia non Infettiva Istituto Superiore di Sanità, Roma, Italy
,
L. Tentori Laboratorio di Patologia non Infettiva Istituto Superiore di Sanità, Roma, Italy
,
C. Omodei Zorini Centro per le Microcitemie, Ospedali Riuniti di Reggio, Calabria, Italy
,
E. Lamberti Centro per le Microcitemie, Ospedali Riuniti di Reggio, Calabria, Italy
,
A. Palazzolo Centro per le Microcitemie, Ospedali Riuniti di Reggio, Calabria, Italy
&
D. Lanzo Centro per le Microcitemie, Ospedali Riuniti di Reggio, Calabria, Italy
 show all
Pages 1-17 | Received 07 Feb 1980, Accepted 28 May 1980, Published online: 07 Jul 2009

Citations (7)

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Mehdi Haghi, Abbas A. Hosseinpour Feizi, Cornelis L. Harteveld, Nasser Pouladi & Mohammad A. Hosseinpour Feizi. (2009) Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family. Hemoglobin 33:1, pages 75-80.
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Articles from other publishers (6)

Nahil Hassan Mahmoud Ahmed & Mei I Lai. (2022) The Novel Role of the B-Cell Lymphoma/Leukemia 11A (BCL11A) Gene in β-Thalassaemia Treatment. Cardiovascular & Hematological Disorders-Drug Targets 22:4, pages 226-236.
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Ha Ly Thi Thanh, Huong Le Thi Thanh, Long Hoang Luong, Thinh Huy Tran, Su-Ching Liu, Hai Nam Truong, Thanh Van Ta, The - Hung Bui & Van Khanh Tran. (2018) Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion. Taiwanese Journal of Obstetrics and Gynecology 57:3, pages 435-441.
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C Altay & A Gurgey. (1985) Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.. Journal of Medical Genetics 22:3, pages 205-212.
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A. Giampaolo, F. Mavilio, N. M. Sposi, A. Car�, A. Massa, L. Cianetti, M. Petrini, R. Russo, M. D. Cappellini & M. Marinucci. (1984) Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal ?-gene expression in association with ? thalassemia and linkage relationship with the ?-globin gene cluster. Human Genetics 66:2-3, pages 151-156.
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A. Giampaolo, F. Mavilio, A. Massa, M. Gabbianelli, R. Guerriero, N. M. Sposi, A. Caré, P. Cianciulli, L. Tentori & M. Marinucci. (2008) Molecular heterogeneity of beta thalassaemia in the Italian population. British Journal of Haematology 56:1, pages 79-85.
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G. Schilirò, L. Pavone, M. A. Romeo, A. Russo, S. Musumeci, G. Russo & John M. Opitz. (2005) Unusual combination of genetic defects in a Sicilian boy: Gγ Aγ δβ thalassemia, Gγ Aγ heterocellular HPFH, βº thalassemia, and albinism. American Journal of Medical Genetics 15:2, pages 225-231.
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