Y279c mutation noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases18

Noonan Syndrome LEOPARD Syndrome Syndrome Costello Syndrome Facies Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Abnormalities, Multiple Failure to Thrive Cherubism Skin Abnormalities Craniofacial Abnormalities Ectodermal Dysplasia Bezoars Heart Defects, Congenital Leukemia, Myelomonocytic, Juvenile Cardiomyopathy, Hypertrophic Neurofibromatosis 1

Chemicals and Drugs5

Protein Tyrosine Phosphatase, Non-Receptor Type 11 SOS1 Protein Protein Tyrosine Phosphatases ras Proteins Intracellular Signaling Peptides and Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment4

Facies DNA Mutational Analysis Pedigree Diagnostic Techniques, Endocrine

Phenomena and Processes8

Mutation Mutation, Missense Point Mutation Germ-Line Mutation Phenotype Sexual Development Genes, Neurofibromatosis 1 Exons

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes

Noonan Syndrome LEOPARD Syndrome Protein Tyrosine Phosphatase, Non-Receptor Type 11 SOS1 Protein Syndrome Mutation Costello Syndrome Mutation, Missense Facies Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Eyebrows Point Mutation Abnormalities, Multiple Germ-Line Mutation Failure to Thrive DNA Mutational Analysis Protein Tyrosine Phosphatases Cherubism Skin Abnormalities Craniofacial Abnormalities Phenotype Ectodermal Dysplasia Sexual Development Bezoars Genes, Neurofibromatosis 1 Heart Defects, Congenital Leukemia, Myelomonocytic, Juvenile Cardiomyopathy, Hypertrophic ras Proteins Pedigree Diagnostic Techniques, Endocrine Neurofibromatosis 1 Intracellular Signaling Peptides and Proteins Exons

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