Pediatric autosomal dominant noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases19

Noonan Syndrome LEOPARD Syndrome Syndrome Costello Syndrome Facies Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Abnormalities, Multiple Polycystic Kidney, Autosomal Dominant Failure to Thrive Cherubism Ectodermal Dysplasia Skin Abnormalities Craniofacial Abnormalities Bezoars Heart Defects, Congenital Neurofibromatosis 1 Leukemia, Myelomonocytic, Juvenile 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 Equipment4

Facies Pedigree DNA Mutational Analysis Diagnostic Techniques, Endocrine

Phenomena and Processes7

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

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

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