Search Results (39)

MatchTypeWhy
ClinGen's RASopathy Expert Panel consensus methods for variant interpretation.Academic Article Why?
Defining RASopathy.Academic Article Why?
Localized Hypertrophic Neuropathy as a Neoplastic Manifestation of KRAS-Mediated RASopathy.Academic Article Why?
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients.Academic Article Why?
Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencing.Academic Article Why?
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis.Academic Article Why?
Advancing RAS/RASopathy therapies: An NCI-sponsored intramural and extramural collaboration for the study of RASopathies.Academic Article Why?
Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?Academic Article Why?
KrasP34R and KrasT58I mutations induce distinct RASopathy phenotypes in mice.Academic Article Why?
Risk of Sudden Death in Patients With RASopathy Hypertrophic Cardiomyopathy.Academic Article Why?
A review of craniofacial and dental findings of the RASopathies.Academic Article Why?
A shared molecular mechanism underlies the human rasopathies Legius syndrome and Neurofibromatosis-1.Academic Article Why?
Autism traits in the RASopathies.Academic Article Why?
Cutaneous mosaic RASopathies associated with rhabdomyosarcoma.Academic Article Why?
Expansion of the RASopathies.Academic Article Why?
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