Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/95943
Type: Artigo de periódico
Title: Molecular Identification Of Hereditary Persistence Of Fetal Hemoglobin Type 2 (hpfh Type 2) In Patients From Brazil
Author: Goncalves M.S.
Fahel S.
Figueiredo M.S.
Kimura E.J.
Nechtman F.
Stoming T.A.
Arruda V.R.
Saad S.T.O.
Costa F.F.
Abstract: The HPFH deletion type 2 was first described in a patient from Ghana and is characterized by a large deletion of approximately 105 kb extension. We report here the results obtained in studying a black Brazilian patient who presented an association of β-thalassemia and HPFH type 2, using a PCR strategy for detection of the breakpoint region. This procedure allows a rapid molecular identification of this condition and is a reliable procedure for screening patients with a hematological picture of HPFH deletion types.
Editor: 
Rights: fechado
Identifier DOI: 10.1007/s002770050050
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0028959736&partnerID=40&md5=f192cde00c0095b6b6fcdaa3b23df0c0
Date Issue: 1995
Appears in Collections:Unicamp - Artigos e Outros Documentos

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