Gene in cowden. Medical search. Frequent questions

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Anatomy2

Chromosomes, Human, Pair 10 Cerebellar Cortex

Organisms2

Caliciviridae Rotavirus

Diseases12

Hamartoma Syndrome, Multiple Intestinal Polyposis Proteus Syndrome Neoplastic Syndromes, Hereditary Polyps Arteriovenous Malformations Syndrome Thyroid Neoplasms Neoplasms, Multiple Primary Breast Neoplasms Hypertrophy Genetic Predisposition to Disease

Chemicals and Drugs4

PTEN Phosphohydrolase Phosphoric Monoester Hydrolases Tumor Suppressor Proteins Protein Tyrosine Phosphatases

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

DNA Mutational Analysis Pedigree

Phenomena and Processes7

Germ-Line Mutation Chromosomes, Human, Pair 10 Genes, Tumor Suppressor Loss of Heterozygosity Mutation Phenotype Genetic Predisposition to Disease

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

Hamartoma Syndrome, Multiple PTEN Phosphohydrolase Phosphoric Monoester Hydrolases Germ-Line Mutation Chromosomes, Human, Pair 10 Intestinal Polyposis Tumor Suppressor Proteins Proteus Syndrome Neoplastic Syndromes, Hereditary Polyps Caliciviridae Arteriovenous Malformations Syndrome Thyroid Neoplasms Genes, Tumor Suppressor DNA Mutational Analysis Pedigree Cerebellar Cortex Neoplasms, Multiple Primary Loss of Heterozygosity Rotavirus Breast Neoplasms Protein Tyrosine Phosphatases Hypertrophy Mutation Phenotype Genetic Predisposition to Disease

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