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Hemoglobin
international journal for hemoglobin research
Volume 20, 1996 - Issue 2
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Original Article

Hereditary Hemoglobinopathies in a Population from so

M. F. Sonati Department of Clinical Pathology, School of Medical Sciences State University of Campinas-UNICAMP, Campinas, SP, Brazil
,
E. M. Kimura Department of Clinical Pathology, School of Medical Sciences State University of Campinas-UNICAMP, Campinas, SP, Brazil
,
H. Z. W. Grotto Department of Clinical Pathology, School of Medical Sciences State University of Campinas-UNICAMP, Campinas, SP, Brazil
,
S. A. Gervasio Department of Clinical Pathology, School of Medical Sciences State University of Campinas-UNICAMP, Campinas, SP, Brazil
&
F. F. Costa Department of Clinical Medicine, School of Medical Sciences State University of Campinas-UNICAMP, Campinas, SP, Brazil
Pages 175-179 | Received 13 Jul 1995, Accepted 28 Mar 1996, Published online: 07 Jul 2009

Citations (9)

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Read on this site (1)

Nadia M. Silva, Cinira S. Soledade, Fernando F. Costa & Maria F. Sonati. (2002) α-THALASSEMIA DOES NOT SIGNIFICANTLY CONTRIBUTE TO THE LOW MCV LEVEL OF Hb C TRAIT. Hemoglobin 26:3, pages 305-309.
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Articles from other publishers (8)

ZuhairAbd Ali Al-Barazanchi, SubehSalim Abdulateef, MeaadKadhum Hassan & RawshanZuhair Jaber. (2019) Double heterozygosity for hemoglobin S and D Punjab in Basra, Iraq: A Clinical and hematological study of 42 patients. Journal of Applied Hematology 10:4, pages 134.
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Aline Menezes Carlos, Renata Andréia Volpe Souza, Bruna Maria Bereta de Souza, Gilberto de Araujo Pereira, Sebastião Tostes Júnior, Paulo Roberto Juliano Martins & Helio Moraes-Souza. (2015) Hemoglobinopathies in newborns in the southern region of the Triângulo Mineiro, Brazil. Cross-sectional study. Sao Paulo Medical Journal 133:5, pages 439-444.
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Lidiane de Souza Torres, Jéssika Viviani Okumura, Danilo Grünig Humberto da Silva & Claudia Regina Bonini-Domingos. (2015) Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis. Revista Brasileira de Hematologia e Hemoterapia 37:2, pages 120-126.
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S.B. Jorge, M.B. Melo, F.F. Costa & M.F. Sonati. (2003) Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism. Brazilian Journal of Medical and Biological Research 36:11, pages 1471-1474.
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K.Y. Fertrin, M.S. Gonçalves, S.T.O. Saad & F.F. Costa. (2002) Frequencies of UDP‐glucuronosyltransferase 1 ( UGT1A 1) gene promoter polymorphisms among distinct ethnic groups from Brazil . American Journal of Medical Genetics 108:2, pages 117-119.
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M.R.S.C. Wenning, E.M. Kimura, F.F. Costa, S.T.O. Saad, S. Gervásio, S.B. de Jorge, E. Borges, N.M. Silva & M.F. Sonati. (2000) alpha-Globin genes: thalassemic and structural alterations in a Brazilian population. Brazilian Journal of Medical and Biological Research 33:9, pages 1041-1045.
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Francisco M. Salzano. (2000) Permanence or change? The meaning of genetic variation. Proceedings of the National Academy of Sciences 97:10, pages 5317-5321.
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Silvana Bordin, Juliana T. Martins, Marilda S. Gonçalves, Mônica B. Melo, Sara T. O. Saad & Fernando F. Costa. (1998) Haplotype analysis andAγ gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin. American Journal of Hematology 58:1, pages 49-54.
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