First report of εγδβ0-thalassemia in a Brazilian family-Reference-Cited by-同舟云学术

First report of εγδβ0-thalassemia in a Brazilian family

Published:2018-05-31 Issue:5 Volume:40 Page:e96-e98
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Ferreira R. D.¹,Mota N. O.¹,Pedroso G. A.¹,Kimura E. M.¹,Geraldo A. P. M.²,Santos M. N. N.¹,Costa F. F.³,Sonati M. F.¹^ORCID

Affiliation:

1. Department of Clinical Pathology; School of Medical Sciences; State University of Campinas - UNICAMP; Campinas SP Brazil

2. Integrated Center for Pediatric Hematology/Oncology Research (CIPOI); School of Medical Sciences; State University of Campinas- UNICAMP; Campinas SP Brazil

3. Hematology and Hemotherapy Center; UNICAMP; Campinas SP Brazil

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12863/fullpdf

Reference19 articles.

1. A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia;Shalev;Eur J Haematol,2013

2. Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements;Phylipsen;Hum Mutat,2012

3. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α and β thalassaemia characterized by high resolution multiplex ligation-dependent probe amplification;Harteveld;J Med Genet,2005

4. A novel deletion causing (epsilon gamma delta beta) degrees thalassaemia in a Chilean family;Game;Br J Haematol,2003

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