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: Blackwell Publishing

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

Document Type: Correspondence

DOI: 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

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