Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements-Reference-Cited by-同舟云学术

Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements

Published:2011-10-31 Issue:1 Volume:33 Page:272-280
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Phylipsen Marion,Chaibunruang Attawut,Vogelaar Ingrid P.,Balak Jeetindra R. A.,Schaap Rianne A. C.,Ariyurek Yavuz,Fucharoen Supan,den Dunnen Johan T.,Giordano Piero C.,Bakker Egbert,Harteveld Cornelis L.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21612/fullpdf

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5. Locus assignment of human alpha globin mutations by selective amplification and direct sequencing;Dode;Br J Haematol,1990

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