Short stature pathway noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases24

Noonan Syndrome LEOPARD Syndrome Syndrome Growth Disorders Dwarfism Facies Costello Syndrome Abnormalities, Multiple Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Failure to Thrive Turner Syndrome Craniofacial Abnormalities Skin Abnormalities Cherubism Heart Defects, Congenital Ectodermal Dysplasia Bezoars Osteochondrodysplasias Leukemia, Myelomonocytic, Juvenile Neurofibromatosis 1 Dwarfism, Pituitary Cardiomyopathy, Hypertrophic Bone Diseases, Developmental

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 Equipment5

Facies Body Height Age Determination by Skeleton Diagnostic Techniques, Endocrine DNA Mutational Analysis

Phenomena and Processes7

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

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 Growth Disorders Dwarfism Facies Costello Syndrome Abnormalities, Multiple Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Eyebrows Body Height Failure to Thrive Turner Syndrome Craniofacial Abnormalities Skin Abnormalities Protein Tyrosine Phosphatases Cherubism Mutation Age Determination by Skeleton Heart Defects, Congenital Ectodermal Dysplasia Sexual Development Bezoars Germ-Line Mutation Phenotype Genes, Neurofibromatosis 1 Osteochondrodysplasias Leukemia, Myelomonocytic, Juvenile Neurofibromatosis 1 Diagnostic Techniques, Endocrine Dwarfism, Pituitary ras Proteins Mutation, Missense Cardiomyopathy, Hypertrophic Bone Diseases, Developmental Intracellular Signaling Peptides and Proteins DNA Mutational Analysis

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