Fmtc germline mutations multiple endocrine neoplasia type 1. Medical search. Frequent questions

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Anatomy11

Chromosomes, Human, Pair 11 Parathyroid Glands Chromosomes, Human, Pair 10 Thyroid Gland Endocrine Glands Endocrine System Adrenal Glands 3T3 Cells Pancreas PC12 Cells Germ Cells

Diseases53

Multiple Endocrine Neoplasia Type 1 Multiple Endocrine Neoplasia Type 2a Multiple Endocrine Neoplasia Type 2b Multiple Endocrine Neoplasia Carcinoma, Medullary Gastrinoma Pheochromocytoma Adrenal Gland Neoplasms Hyperparathyroidism, Primary Parathyroid Neoplasms Thyroid Neoplasms Zollinger-Ellison Syndrome Hyperparathyroidism Pituitary Neoplasms Insulinoma Neuroma Angiofibroma Pancreatic Neoplasms Bone Demineralization, Pathologic Adenoma Neuroendocrine Tumors von Hippel-Lindau Disease Adenoma, Islet Cell Hirschsprung Disease Paraganglioma Endocrine Gland Neoplasms Duodenal Neoplasms Carcinoid Tumor Glucagonoma Neoplastic Syndromes, Hereditary Ganglioneuroma Prolactinoma Vipoma Lipoma Acromegaly Parathyroid Diseases Neoplasms, Multiple Primary Syndrome Growth Hormone-Secreting Pituitary Adenoma Hyperplasia Thymus Neoplasms Hypercalcemia Genetic Predisposition to Disease Endocrine System Diseases Carcinoma Paraganglioma, Extra-Adrenal Cell Transformation, Neoplastic Colorectal Neoplasms, Hereditary Nonpolyposis Adenomatous Polyposis Coli Hamartoma Syndrome, Multiple Adrenal Cortex Neoplasms Carcinoma, Neuroendocrine Cervical Intraepithelial Neoplasia

Chemicals and Drugs22

Proto-Oncogene Proteins c-ret Proto-Oncogene Proteins Receptor Protein-Tyrosine Kinases Drosophila Proteins Calcitonin Metanephrine Cyclin-Dependent Kinase Inhibitor p18 Normetanephrine Neoplasm Proteins DNA, Neoplasm Gastrins Codon Parathyroid Hormone Genetic Markers Cyclin-Dependent Kinase Inhibitor p27 Octreotide Somatostatin Succinate Dehydrogenase DNA MutS Homolog 2 Protein Endocrine Disruptors BRCA2 Protein

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Pedigree Thyroidectomy Genetic Testing Parathyroidectomy DNA Mutational Analysis Polymerase Chain Reaction Pancreatectomy Adrenalectomy Heterozygote Detection Pancreaticoduodenectomy Sequence Analysis, DNA Chromosome Mapping Thymectomy Tomography, X-Ray Computed Follow-Up Studies Immunohistochemistry Genetic Association Studies X-Ray Therapy Magnetic Resonance Imaging Reverse Transcriptase Polymerase Chain Reaction Retrospective Studies Amino Acid Substitution

Phenomena and Processes30

Germ-Line Mutation Chromosomes, Human, Pair 11 Mutation Mutation, Missense Point Mutation Loss of Heterozygosity Proto-Oncogenes Polymorphism, Single-Stranded Conformational Chromosomes, Human, Pair 10 Heterozygote Exons Frameshift Mutation Phenotype Genes, Tumor Suppressor Codon Base Sequence Alleles Genetic Predisposition to Disease Gene Deletion Genetic Markers Genotype Genetic Linkage Polymorphism, Genetic Polymorphism, Restriction Fragment Length Genes, BRCA1 Gene Expression Regulation, Neoplastic Microsatellite Repeats Signal Transduction Amino Acid Substitution Genes, BRCA2

Disciplines and Occupations1

Immunohistochemistry

Information Science2

Base Sequence Molecular Sequence Data

Named Groups1

Asian Continental Ancestry Group

Health Care4

Genetic Testing Family Health Follow-Up Studies Retrospective Studies

Geographicals1

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care Geographicals

Multiple Endocrine Neoplasia Type 1 Multiple Endocrine Neoplasia Type 2a Multiple Endocrine Neoplasia Type 2b Multiple Endocrine Neoplasia Proto-Oncogene Proteins c-ret Carcinoma, Medullary Germ-Line Mutation Gastrinoma Pheochromocytoma Adrenal Gland Neoplasms Hyperparathyroidism, Primary Parathyroid Neoplasms Thyroid Neoplasms Zollinger-Ellison Syndrome Proto-Oncogene Proteins Hyperparathyroidism Pituitary Neoplasms Insulinoma Pedigree Receptor Protein-Tyrosine Kinases Neuroma Angiofibroma Pancreatic Neoplasms Chromosomes, Human, Pair 11 Bone Demineralization, Pathologic Thyroidectomy Adenoma Neuroendocrine Tumors Mutation Genetic Testing von Hippel-Lindau Disease Drosophila Proteins Parathyroidectomy Mutation, Missense Calcitonin Adenoma, Islet Cell Hirschsprung Disease Paraganglioma Endocrine Gland Neoplasms Metanephrine Duodenal Neoplasms Carcinoid Tumor Point Mutation DNA Mutational Analysis Glucagonoma Parathyroid Glands Neoplastic Syndromes, Hereditary Ganglioneuroma Prolactinoma Loss of Heterozygosity Proto-Oncogenes Cyclin-Dependent Kinase Inhibitor p18 Polymorphism, Single-Stranded Conformational Vipoma Chromosomes, Human, Pair 10 Heterozygote Normetanephrine Exons Neoplasm Proteins Frameshift Mutation Phenotype Lipoma Acromegaly Polymerase Chain Reaction Parathyroid Diseases Neoplasms, Multiple Primary Syndrome DNA, Neoplasm Pancreatectomy Genes, Tumor Suppressor Gastrins Adrenalectomy Codon Growth Hormone-Secreting Pituitary Adenoma Hyperplasia Base Sequence Heterozygote Detection Thymus Neoplasms Alleles Pancreaticoduodenectomy Hypercalcemia Family Health Genetic Predisposition to Disease Gene Deletion Molecular Sequence Data Parathyroid Hormone Genetic Markers Thyroid Gland Sequence Analysis, DNA Chromosome Mapping Thymectomy Endocrine System Diseases Genotype Cyclin-Dependent Kinase Inhibitor p27 Octreotide Endocrine Glands Carcinoma Endocrine System Genetic Linkage Paraganglioma, Extra-Adrenal

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