The Ivs-1-110 (G→T) and Codon 39 (C→T) β-Thalassemia Mutations in Association with α-Thal-2 (−3.7 Kb) and Hb Hasharon [α47(CE5)Asp→His] in a Brazilian Patient

F. F. Costa Department of Clinical Medicine, School of edical Sciences State University of Campinas-UNICAMP, SP, Brazil

M. S. Figueredo Department of Clinical Medicine, School of edical Sciences State University of Campinas-UNICAMP, SP, Brazil

M. F. Sonati Department of Clinical Pathology, School of edical Sciences State University of Campinas-UNICAMP, SP, Brazil

E. M. Kimura Department of Clinical Pathology, School of edical Sciences State University of Campinas-UNICAMP, SP, Brazil

C. S. B. Martins Department of Medical Genetics, School of edical Sciences State University of Campinas-UNICAMP, SP, Brazil

Citations (4)

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (2)

Mönica Barbosa De MELO, Irene Lorand-Metze, Carmen Silvia Passos Lima, Sara Terezinha Ohlala Saad & Fernando Ferreira Costa. (1997) “N-ras Gene Point Mutations in Brazilian Acute Myelogenous Leukemia Patients Correlate with a Poor Prognosiss”. Leukemia & Lymphoma 24:3-4, pages 309-317.
Read now

M. F. Sonati, E. M. Kimura, H. Z. W. Grotto, S. A. Gervasio & F. F. Costa. (1996) Hereditary Hemoglobinopathies in a Population from so. Hemoglobin 20:2, pages 175-179.
Read now

Articles from other publishers (2)

Elza Miyuki Kimura, Denise Madureira Oliveira, Susan Elisabeth Jorge, Daniela Maria Ribeiro, Tânia Regina Zaccariotto, Magnun Nueldo Nunes Santos, Vanessa Almeida, Dulcinéia Martins Albuquerque, Fernando Ferreira Costa & Maria de Fátima Sonati. (2015) Investigating alpha-globin structural variants: a retrospective review of 135,000 Brazilian individuals. Revista Brasileira de Hematologia e Hemoterapia 37:2, pages 103-108.
Crossref

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.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

The Ivs-1-110 (G→T) and Codon 39 (C→T) β-Thalassemia Mutations in Association with α-Thal-2 (−3.7 Kb) and Hb Hasharon [α47(CE5)Asp→His] in a Brazilian Patient

Articles from other publishers (2)

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

The Ivs-1-110 (G→T) and Codon 39 (C→T) β-Thalassemia Mutations in Association with α-Thal-2 (−3.7 Kb) and Hb Hasharon [α47(CE5)Asp→His] in a Brazilian Patient

Citations (4)

Read on this site (2)

Articles from other publishers (2)

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date