Genetic infancy 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 Neurofibromatosis 1 Cardiomyopathy, Hypertrophic

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 Equipment2

Facies Diagnostic Techniques, Endocrine

Phenomena and Processes4

Sexual Development Genes, Neurofibromatosis 1 Germ-Line Mutation Mutation

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

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