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Items: 2

1.
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
Andrew J Makoff, Rachel H Flomen
Genome Biol. 2007; 8(6): R114. Published online 2007 Jun 15. doi: 10.1186/gb-2007-8-6-r114
PMCID:
PMC2394762
AbstractArticlePDF–514K
2.
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region
Yong-hui Jiang, Kekio Wauki, Qian Liu, Jan Bressler, Yanzhen Pan, Catherine D Kashork, Lisa G Shaffer, Arthur L Beaudet
BMC Genomics. 2008; 9: 50. Published online 2008 Jan 28. doi: 10.1186/1471-2164-9-50
PMCID:
PMC2268926
AbstractArticlePDF–831K

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