Noonan SyndromeCostello SyndromeNeurofibromatosis 1Neurofibromatosis 2Genes, Neurofibromatosis 1SyndromeSkin AbnormalitiesFaciesLEOPARD SyndromeAbnormalities, MultipleFailure to ThriveProtein Tyrosine Phosphatase, Non-Receptor Type 11Genes, Neurofibromatosis 2SOS1 ProteinNeurofibromatosesIntellectual DisabilityProto-Oncogene Proteins p21(ras)Neurofibromin 1Germ-Line MutationHeart Defects, CongenitalChondroitin ABC LyaseNeurofibromin 2Loose Anagen Hair SyndromeGenes, rasPulmonary Valve StenosisNeurofibroma, PlexiformTropoelastinEyebrowsMutationEctodermal DysplasiaNeurofibromaCafe-au-Lait SpotsMosaicismBiglycanOptic Nerve Gliomaras ProteinsCraniofacial AbnormalitiesProtein Tyrosine PhosphatasesCherubismLeukemia, Myelomonocytic, JuvenileNerve Sheath NeoplasmsNeurilemmomaPhenotypeBezoarsSexual DevelopmentDiagnostic Techniques, EndocrineDown SyndromeChondroitin SulfatesMetabolic Syndrome XIntracellular Signaling Peptides and ProteinsDNA Mutational AnalysisCardiomyopathy, Hypertrophic