Amino 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 Skin Abnormalities Craniofacial 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 Equipment3

Facies DNA Mutational Analysis Diagnostic Techniques, Endocrine

Phenomena and Processes7

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

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

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