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Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes
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* Corresponding author: Andrew J Makoff a.makoff@iop.kcl.ac.uk
Genome Biology 2007, 8:R114 doi:10.1186/gb-2007-8-6-r114