A new deletion defect leading to ?-thalassaemia in a large Dutch Caucasian family
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2006.06475.x/fullpdf
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3. Caracterización molecular de dos nuevas mutaciones de α° talasemia en 2 familias españolas (mutación --ED y --GP);Medicina Clínica;2011-05
4. Characterisation of the British α0-thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada;British Journal of Haematology;2009-10
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