Mutations 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 Craniofacial Abnormalities Skin Abnormalities Cherubism 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 Processes9

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

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