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The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway
- Stevenson, David A;
- Schill, Lisa;
- Schoyer, Lisa;
- Andresen, Brage S;
- Bakker, Annette;
- Bayrak-Toydemir, Pinar;
- Burkitt-Wright, Emma;
- Chatfield, Kathryn;
- Elefteriou, Florent;
- Elgersma, Ype;
- Fisher, Michael J;
- Franz, David;
- Gelb, Bruce D;
- Goriely, Anne;
- Gripp, Karen W;
- Hardan, Antonio Y;
- Keppler-Noreuil, Kim M;
- Kerr, Bronwyn;
- Korf, Bruce;
- Leoni, Chiara;
- McCormick, Frank;
- Plotkin, Scott R;
- Rauen, Katherine A;
- Reilly, Karlyne;
- Roberts, Amy;
- Sandler, Abby;
- Siegel, Dawn;
- Walsh, Karin;
- Widemann, Brigitte C
- et al.
Published Web Location
https://doi.org/10.1002/ajmg.a.37723Abstract
The 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. © 2016 Wiley Periodicals, Inc.
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