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The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway

dc.contributor.authorStevenson, David A.
dc.contributor.authorSchill, Lisa
dc.contributor.authorSchoyer, Lisa
dc.contributor.authorAndresen, Brage S.
dc.contributor.authorBakker, Annette
dc.contributor.authorBayrak-Toydemir, Pinar
dc.contributor.authorBurkitt-Wright, Emma
dc.contributor.authorChatfield, Kathryn
dc.contributor.authorElefteriou, Florent
dc.contributor.authorElgersma, Ype
dc.contributor.authorFisher, Michael J.
dc.contributor.authorFranz, David
dc.contributor.authorGelb, Bruce D.
dc.contributor.authorGoriely, Anne
dc.contributor.authorGripp, Karen W.
dc.contributor.authorHardan, Antonio Y.
dc.contributor.authorKeppler-Noreuil, Kim M.
dc.contributor.authorKerr, Bronwyn
dc.contributor.authorKorf, Bruce
dc.contributor.authorLeoni, Chiara
dc.contributor.authorMcCormick, Frank
dc.contributor.authorPlotkin, Scott Randall
dc.contributor.authorRauen, Katherine A.
dc.contributor.authorReilly, Karlyne
dc.contributor.authorRoberts, Amy Elizabeth
dc.contributor.authorSandler, Abby
dc.contributor.authorSiegel, Dawn
dc.contributor.authorWalsh, Karin
dc.contributor.authorWidemann, Brigitte C.
dc.date.accessioned2017-05-15T17:13:01Z
dc.date.issued2016
dc.identifier.citationStevenson, David A., Lisa Schill, Lisa Schoyer, Brage S. Andresen, Annette Bakker, Pinar Bayrak-Toydemir, Emma Burkitt-Wright, et al. 2016. “The Fourth International Symposium on Genetic Disorders of the Ras/MAPK Pathway.” American Journal of Medical Genetics Part A 170 (8) (May 7): 1959–1966. Portico. doi:10.1002/ajmg.a.37723.en_US
dc.identifier.issn1552-4825en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:32674685
dc.description.abstractThe RASopathies are a group of disorders due to variations of genes associated with the Ras/MAPK pathway. Some of the RASopathies include neurofibromatosis type 1 (NF1), Noonan syndrome, Noonan syndrome with multiple lentigines, cardiofaciocutaneous (CFC) syndrome, Costello syndrome, Legius syndrome, and capillary malformation–arteriovenous malformation (CM-AVM) syndrome. In combination, the RASopathies are a frequent group of genetic disorders. This report summarizes the proceedings of the 4th International Symposium on Genetic Disorders of the Ras/MAPK pathway and highlights gaps in the field.en_US
dc.language.isoen_USen_US
dc.publisherWiley-Blackwellen_US
dc.relation.isversionof10.1002/ajmg.a.37723en_US
dc.relation.hasversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945362/en_US
dash.licenseOAP
dc.titleThe Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathwayen_US
dc.typeJournal Articleen_US
dc.description.versionAccepted Manuscripten_US
dc.relation.journalAmerican Journal of Medical Genetics Part Aen_US
dash.depositing.authorPlotkin, Scott Randall
dc.date.available2017-05-15T17:13:01Z
dc.identifier.doi10.1002/ajmg.a.37723*
dash.authorsorderedfalse
dash.contributor.affiliatedRoberts, Amy
dash.contributor.affiliatedPlotkin, Scott


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