Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification.

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Published in J Med Genet on May 13, 2005

Authors

C L Harteveld1, A Voskamp, M Phylipsen, N Akkermans, J T den Dunnen, S J White, P C Giordano

Author Affiliations

1: Center of Human and Clinical Genetics, Leiden University Medical Center, The Netherlands. C.L.Harteveld@LUMC.nl

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