1968 multiple endocrine neoplasia type 2a. Medical search. Frequent questions

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Anatomy10

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

Diseases49

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

Chemicals and Drugs18

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

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

Phenomena and Processes25

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

Disciplines and Occupations1

Immunohistochemistry

Information Science2

Base Sequence Molecular Sequence Data

Named Groups1

Asian Continental Ancestry Group

Health Care3

Genetic Testing Family Health Follow-Up 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 Gastrinoma Pheochromocytoma Adrenal Gland Neoplasms Hyperparathyroidism, Primary Parathyroid Neoplasms Zollinger-Ellison Syndrome Germ-Line Mutation Thyroid Neoplasms Hyperparathyroidism Proto-Oncogene Proteins Pituitary Neoplasms Insulinoma Neuroma Receptor Protein-Tyrosine Kinases Angiofibroma Pancreatic Neoplasms Pedigree Chromosomes, Human, Pair 11 Bone Demineralization, Pathologic Thyroidectomy Neuroendocrine Tumors Adenoma Parathyroidectomy Adenoma, Islet Cell Calcitonin Endocrine Gland Neoplasms Metanephrine Duodenal Neoplasms Carcinoid Tumor von Hippel-Lindau Disease Hirschsprung Disease Glucagonoma Drosophila Proteins Genetic Testing Parathyroid Glands Ganglioneuroma Prolactinoma Paraganglioma Mutation Proto-Oncogenes Loss of Heterozygosity Cyclin-Dependent Kinase Inhibitor p18 Vipoma Chromosomes, Human, Pair 10 Normetanephrine DNA Mutational Analysis Neoplastic Syndromes, Hereditary Mutation, Missense Lipoma Acromegaly Parathyroid Diseases Polymorphism, Single-Stranded Conformational Neoplasm Proteins Pancreatectomy Point Mutation Gastrins Adrenalectomy Heterozygote Neoplasms, Multiple Primary Hyperplasia Thymus Neoplasms Phenotype Genes, Tumor Suppressor Growth Hormone-Secreting Pituitary Adenoma Exons Syndrome Pancreaticoduodenectomy Hypercalcemia Polymerase Chain Reaction DNA, Neoplasm Codon Parathyroid Hormone Thyroid Gland Thymectomy Heterozygote Detection Endocrine System Diseases Octreotide Endocrine Glands Endocrine System Cyclin-Dependent Kinase Inhibitor p27 Frameshift Mutation Genetic Markers Adrenal Glands Chromosome Mapping Gene Deletion Carcinoma Tomography, X-Ray Computed Base Sequence Japan Alleles Family Health Somatostatin Genetic Linkage 3T3 Cells

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