Germline mutations of men 1. Medical search. Frequent questions

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Anatomy7

Germ Cells Cell Line Micronucleus, Germline Stem Cells Cells, Cultured Chromosomes, Human, Pair 9 Ovary

Organisms9

Caenorhabditis elegans Drosophila melanogaster Drosophila Animals, Genetically Modified Escherichia coli Mice, Mutant Strains Mice, Transgenic Saccharomyces cerevisiae Mice, Inbred C57BL

Diseases69

Neoplastic Syndromes, Hereditary Colorectal Neoplasms, Hereditary Nonpolyposis Paraganglioma Hamartoma Syndrome, Multiple Genetic Predisposition to Disease Adenomatous Polyposis Coli Li-Fraumeni Syndrome Peutz-Jeghers Syndrome Multiple Endocrine Neoplasia Type 2a von Hippel-Lindau Disease Intestinal Polyposis Pheochromocytoma Paraganglioma, Extra-Adrenal Syndrome Noonan Syndrome Costello Syndrome Microsatellite Instability Leiomyomatosis Carcinoma, Medullary Breast Neoplasms Adrenal Gland Neoplasms Ovarian Neoplasms Multiple Endocrine Neoplasia Type 1 Colorectal Neoplasms Neoplasms, Multiple Primary Adenoma Abnormalities, Multiple Melanoma Birt-Hogg-Dube Syndrome Thyroid Neoplasms Retinoblastoma Hemangioblastoma Retinal Neoplasms Facies Skin Neoplasms LEOPARD Syndrome Sebaceous Gland Neoplasms Hirschsprung Disease Multiple Endocrine Neoplasia Type 2b Endometrial Neoplasms Craniofacial Abnormalities Growth Hormone-Secreting Pituitary Adenoma Ectodermal Dysplasia Neoplasms Intestinal Polyps Neurofibromatosis 1 Skin Abnormalities Kidney Neoplasms Hereditary Breast and Ovarian Cancer Syndrome Abdominal Neoplasms Breast Neoplasms, Male Adenocarcinoma Neurofibromatoses Dysplastic Nevus Syndrome Stomach Neoplasms Multiple Endocrine Neoplasia Cell Transformation, Neoplastic Pancreatic Neoplasms Carcinoma Carotid Body Tumor Prolactinoma Adrenal Cortex Neoplasms Carcinoma, Renal Cell Gastrointestinal Neoplasms Polyps Rhabdoid Tumor Genomic Instability Pituitary Neoplasms Polycythemia

Chemicals and Drugs57

MutS Homolog 2 Protein BRCA2 Protein Proto-Oncogene Proteins c-ret BRCA1 Protein Succinate Dehydrogenase DNA, Neoplasm Nuclear Proteins Adaptor Proteins, Signal Transducing Codon, Nonsense Fumarate Hydratase DNA-Binding Proteins Neoplasm Proteins Proto-Oncogene Proteins Codon Tumor Suppressor Proteins Drosophila Proteins Transcription Factors DNA Primers Carrier Proteins PTEN Phosphohydrolase Von Hippel-Lindau Tumor Suppressor Protein DNA Proto-Oncogene Proteins B-raf DNA Repair Enzymes Tumor Suppressor Protein p53 Protein-Serine-Threonine Kinases Caenorhabditis elegans Proteins Genetic Markers Adenomatous Polyposis Coli Protein Membrane Proteins Mutant Proteins Cyclin-Dependent Kinase Inhibitor p16 RNA Splice Sites DNA Glycosylases Phosphoric Monoester Hydrolases RNA, Messenger Receptor Protein-Tyrosine Kinases Proteins Electron Transport Complex II Immunoglobulin Variable Region ras Proteins Adenosine Triphosphatases Cadherins Californium DNA Transposable Elements Immunoglobulin Heavy Chains Tumor Suppressor Protein p14ARF Receptors, Thyrotropin Intracellular Signaling Peptides and Proteins Bone Morphogenetic Protein Receptors, Type I Dexfenfluramine Ubiquitin-Protein Ligases DNA, Mitochondrial Bacterial Proteins Checkpoint Kinase 2 Smad4 Protein Bone Morphogenetic Protein Receptors, Type II

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

Pedigree DNA Mutational Analysis Genetic Testing Polymerase Chain Reaction Sequence Analysis, DNA Amino Acid Substitution Heterozygote Detection Mutagenesis, Site-Directed Models, Genetic Immunohistochemistry Case-Control Studies Models, Molecular Chromosome Mapping Mutagenesis, Insertional Cohort Studies Facies Risk Factors Cloning, Molecular Sequence Alignment Genetic Association Studies Genetic Complementation Test Transfection Reverse Transcriptase Polymerase Chain Reaction Heteroduplex Analysis Crosses, Genetic Models, Biological Blotting, Southern Gene Targeting Prognosis

Psychiatry and Psychology1

Phenomena and Processes82

Germ-Line Mutation Mutation, Missense Point Mutation Mutation Frameshift Mutation Genes, BRCA1 Exons Heterozygote Genetic Predisposition to Disease Genes, BRCA2 Polymorphism, Single-Stranded Conformational Base Sequence Mutation Rate Alleles DNA Mismatch Repair Phenotype Loss of Heterozygosity Genes, APC Microsatellite Repeats Genotype Penetrance Codon, Nonsense Amino Acid Substitution Sequence Deletion Founder Effect Amino Acid Sequence Microsatellite Instability Genes, p53 Base Pair Mismatch Codon Homozygote Mosaicism Mutagenesis Gene Deletion Polymorphism, Genetic Gene Frequency Genes, p16 Genes, Recessive Genes, Dominant Exome DNA Repair Genes, Tumor Suppressor Oogenesis Protein Structure, Tertiary Genetic Linkage Genetic Variation Introns Polymorphism, Single Nucleotide Promoter Regions, Genetic Sequence Homology, Amino Acid Signal Transduction Genetic Markers Mutagenesis, Insertional Genes, Neurofibromatosis 1 Consanguinity RNA Splice Sites DNA Methylation Suppression, Genetic Transcription, Genetic Genetic Heterogeneity Recombination, Genetic Binding Sites Immunoglobulin Variable Region Heredity Transfection Protein Binding Haploinsufficiency Gene Expression Regulation, Neoplastic Genes, Lethal Gene Expression Regulation, Developmental Haplotypes Gene Rearrangement Gene Silencing Genes, Immunoglobulin Genes, X-Linked DNA Transposable Elements Gene Expression Regulation Plasmids Genomic Instability Spermatogenesis Chromosomes, Human, Pair 9 Cell Differentiation

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups3

Jews Men Asian Continental Ancestry Group

Health Care9

Genetic Testing Age of Onset Family Health Case-Control Studies Genetic Counseling Cohort Studies Risk Factors Age Factors Men's Health

Geographicals2

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Germ-Line Mutation Mutation, Missense Point Mutation Mutation Pedigree DNA Mutational Analysis Neoplastic Syndromes, Hereditary Frameshift Mutation Colorectal Neoplasms, Hereditary Nonpolyposis Genes, BRCA1 MutS Homolog 2 Protein Paraganglioma Exons Genetic Testing BRCA2 Protein Heterozygote Hamartoma Syndrome, Multiple Genetic Predisposition to Disease Adenomatous Polyposis Coli Genes, BRCA2 Germ Cells Polymorphism, Single-Stranded Conformational Base Sequence Li-Fraumeni Syndrome Mutation Rate Alleles Polymerase Chain Reaction DNA Mismatch Repair Molecular Sequence Data Phenotype Loss of Heterozygosity Peutz-Jeghers Syndrome Age of Onset Genes, APC Proto-Oncogene Proteins c-ret Family Health Microsatellite Repeats BRCA1 Protein Succinate Dehydrogenase Sequence Analysis, DNA Multiple Endocrine Neoplasia Type 2a Genotype Penetrance DNA, Neoplasm Nuclear Proteins von Hippel-Lindau Disease Intestinal Polyposis Pheochromocytoma Adaptor Proteins, Signal Transducing Codon, Nonsense Paraganglioma, Extra-Adrenal Fumarate Hydratase Amino Acid Substitution DNA-Binding Proteins Sequence Deletion Syndrome Founder Effect Noonan Syndrome Costello Syndrome Amino Acid Sequence Neoplasm Proteins Microsatellite Instability Leiomyomatosis Proto-Oncogene Proteins Carcinoma, Medullary Breast Neoplasms Adrenal Gland Neoplasms Genes, p53 Ovarian Neoplasms Base Pair Mismatch Multiple Endocrine Neoplasia Type 1 Codon Tumor Suppressor Proteins Homozygote Jews Heterozygote Detection Colorectal Neoplasms Drosophila Proteins Transcription Factors DNA Primers Mosaicism Carrier Proteins Neoplasms, Multiple Primary Mutagenesis Gene Deletion Polymorphism, Genetic PTEN Phosphohydrolase Gene Frequency Genes, p16 Men Von Hippel-Lindau Tumor Suppressor Protein Genes, Recessive Genes, Dominant Exome Caenorhabditis elegans DNA Repair Mutagenesis, Site-Directed DNA Adenoma Family

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