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Items: 3

1.
Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.
D Pfeifer, R Kist, K Dewar, K Devon, E S Lander, B Birren, L Korniszewski, E Back, G Scherer
Am J Hum Genet. 1999 Jul; 65(1): 111–124. doi: 10.1086/302455
PMCID:
PMC1378081
SummaryPDF–515K
2.
Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia
Véronique M. Wunderle, Ricky Critcher, Nicholas Hastie, Peter N. Goodfellow, Andreas Schedl
Proc Natl Acad Sci U S A. 1998 Sep 1; 95(18): 10649–10654. doi: 10.1073/pnas.95.18.10649
PMCID:
PMC27949
AbstractArticlePDF–422K
3.
Functional Dissection of the Enhancer Repertoire in Human Embryonic Stem Cells
Tahsin Stefan Barakat, Florian Halbritter, Man Zhang, André F. Rendeiro, Elena Perenthaler, Christoph Bock, Ian Chambers
Cell Stem Cell. 2018 Aug 2; 23(2): 276–288.e8. doi: 10.1016/j.stem.2018.06.014
PMCID:
PMC6084406
AbstractArticle

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