Family history of the condition 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 Cherubism Craniofacial Abnormalities Skin Abnormalities 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 Processes7

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

Health Care1

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

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

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