Braf mutation noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases20

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 Microsatellite Instability Cardiomyopathy, Hypertrophic Neurofibromatosis 1 Melanoma

Chemicals and Drugs7

Proto-Oncogene Proteins B-raf Protein Tyrosine Phosphatase, Non-Receptor Type 11 SOS1 Protein ras Proteins Protein Tyrosine Phosphatases Proto-Oncogene Proteins c-raf Intracellular Signaling Peptides and Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Facies DNA Mutational Analysis Diagnostic Techniques, Endocrine

Phenomena and Processes10

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

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

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

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