Genotype phenotype noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases20

Noonan Syndrome LEOPARD Syndrome Syndrome Costello Syndrome Facies Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Frasier Syndrome Abnormalities, Multiple Failure to Thrive Cherubism Craniofacial Abnormalities Skin Abnormalities Ectodermal Dysplasia Bezoars Heart Defects, Congenital Leukemia, Myelomonocytic, Juvenile Niemann-Pick Diseases Neurofibromatosis 1 Cardiomyopathy, Hypertrophic

Chemicals and Drugs6

Protein Tyrosine Phosphatase, Non-Receptor Type 11 SOS1 Protein Protein Tyrosine Phosphatases ras Proteins Intracellular Signaling Peptides and Proteins Codon, Nonsense

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Facies DNA Mutational Analysis Pedigree Diagnostic Techniques, Endocrine Genetic Association Studies

Phenomena and Processes11

Phenotype Genotype Mutation Mutation, Missense Sexual Development Genes, Neurofibromatosis 1 Germ-Line Mutation Exons Polymorphism, Genetic Codon, Nonsense Alleles

Health Care1

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

Noonan Syndrome LEOPARD Syndrome Phenotype Protein Tyrosine Phosphatase, Non-Receptor Type 11 Genotype SOS1 Protein Syndrome Mutation Costello Syndrome Facies Loose Anagen Hair Syndrome DNA Mutational Analysis Pulmonary Valve Stenosis Eyebrows Mutation, Missense Frasier Syndrome Abnormalities, Multiple Failure to Thrive Protein Tyrosine Phosphatases Cherubism Craniofacial Abnormalities Skin Abnormalities Pedigree Ectodermal Dysplasia Sexual Development Bezoars Genes, Neurofibromatosis 1 Heart Defects, Congenital Germ-Line Mutation Leukemia, Myelomonocytic, Juvenile Exons Niemann-Pick Diseases Polymorphism, Genetic Diagnostic Techniques, Endocrine ras Proteins Genetic Association Studies Neurofibromatosis 1 Cardiomyopathy, Hypertrophic Age of Onset Intracellular Signaling Peptides and Proteins Codon, Nonsense Alleles

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