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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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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Group
2007
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| Fag: | |
| Online adgang: | 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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