The deletion of SOX8 is not associated with ATR-16 in an HbH family from Brazil

Authors: Bezerra, M. A. C. B.; Araujo, A. S.¹; Phylipsen, M.²; Balak, D.²; Kimura, E. M.³; Oliveira, D. M.³; Costa, F. F.⁴; Sonati, M. F.³; Harteveld, C. L.²

Source: British Journal of Haematology, Volume 142, Number 2, July 2008 , pp. 324-326(3)

Publisher: Wiley-Blackwell

Keywords: HbH; SOX8; mental retardation; ATR-16; multiplex ligation dependent probe amplification

Document Type: Correspondence

DOI: http://dx.doi.org/10.1111/j.1365-2141.2008.07187.x

Affiliations: 1: Haematology and Haemotherapy Centre of Pernambuco - HEMOPE, Recife, Pernambuco, Brazil 2: Haemoglobinopathies Laboratory, Human and Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands 3: Department of Clinical Pathology, State University of Campinas - UNICAMP, Campinas, São Paulo, Brazil., Email: c.l.harteveld@lumc.nl 4: Haematology and Haemotherapy Centre, State University of Campinas - UNICAMP, Campinas, São Paulo, Brazil

Publication date: 2008-07-01

• In this: publication
• By this: publisher
• In this Subject: Pathology
• By this author: Bezerra, M. A. C. B. ;  Araujo, A. S. ;  Phylipsen, M. ;  Balak, D. ;  Kimura, E. M. ;  Oliveira, D. M. ;  Costa, F. F. ;  Sonati, M. F. ;  Harteveld, C. L.

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