Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

BACKGROUND: Noonan syndrome, cardio‐facio‐cutaneous syndrome (CFC) and Costello syndrome constitute a group of developmental disorders with an overlapping pattern of congenital anomalies. Each of these conditions can be caused by germline mutations in key components of the highly conserved Ras‐MAPK...

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Detalhes bibliográficos
Main Authors: Zenker, Martin, Lehmann, Katarina, Schulz, Anna Leana, Barth, Helmut, Hansmann, Dagmar, Koenig, Rainer, Korinthenberg, Rudolf, Kreiss‐Nachtsheim, Martina, Meinecke, Peter, Morlot, Susanne, Mundlos, Stefan, Quante, Anne S, Raskin, Salmo, Schnabel, Dirk, Wehner, Lars‐Erik, Kratz, Christian P, Horn, Denise
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2598066/
https://ncbi.nlm.nih.gov/pubmed/17056636
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.046300
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