Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Monosomy of the human chromosome 6p terminal region results in a variety of congenital malformations that include brain, craniofacial, and organogenesis abnormalities. To examine the genetic basis of these phenotypes, we have carried out an unbiased functional analysis of the syntenic region of the...

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Bibliografische gegevens
Hoofdauteurs: Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, Haines, Heather, McKeone, Richard, Cadman, Matthew, Pieles, Guido, Schneider, Jürgen E., Bhattacharya, Shoumo, Hardy, Andrea, Nolan, Patrick M., Tripodis, Nikos, Depew, Michael J., Chandrasekara, Ramya, Duncan, Gimara, Sharpe, Paul T., Greenfield, Andy, Denny, Paul, Brown, Steve D. M., Ragoussis, Jiannis, Arkell, Ruth M.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: National Academy of Sciences 2005
Onderwerpen:
Biological Sciences
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1194901/
https://ncbi.nlm.nih.gov/pubmed/16109771
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0500584102
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