Incomplete or reduced penetrance penetrance. Medical search. Frequent questions

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Anatomy1

Chromosomes, Human, Pair 19

Organisms2

Mice, Transgenic Mice, Inbred C57BL

Diseases24

Genetic Predisposition to Disease Optic Atrophy, Hereditary, Leber Hirschsprung Disease Genetic Diseases, Inborn Dystonia Musculorum Deformans Syndrome Dystonia Amyloid Neuropathies, Familial Angiomatosis Hemochromatosis Syndactyly Abnormalities, Multiple Craniofacial Abnormalities Retinoblastoma Cardiomyopathy, Hypertrophic, Familial Myoclonus Neoplastic Syndromes, Hereditary Breast Neoplasms Optic Atrophies, Hereditary Dystonic Disorders Retinitis Pigmentosa Paraganglioma, Extra-Adrenal Ovarian Neoplasms Eye Abnormalities

Chemicals and Drugs7

Genetic Markers BRCA2 Protein Proto-Oncogene Proteins c-ret DNA, Mitochondrial RNA, Transfer, Ile Bone Morphogenetic Protein Receptors, Type II Prealbumin

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Pedigree DNA Mutational Analysis Genetic Testing Models, Genetic Chromosome Mapping Heterozygote Detection Crosses, Genetic Likelihood Functions Genetic Association Studies

Psychiatry and Psychology1

Phenomena and Processes30

Penetrance Genes, Dominant Heterozygote Mutation Phenotype Genetic Linkage Genetic Predisposition to Disease Lod Score Alleles Germ-Line Mutation Genotype Genes, BRCA1 Genes, Modifier Founder Effect Haplotypes Homozygote Genes, Recessive Genetic Heterogeneity Gene Frequency Genes, BRCA2 Mutation, Missense Genetic Markers Genetic Variation Polymorphism, Single Nucleotide Epistasis, Genetic Chromosomes, Human, Pair 19 Inheritance Patterns Exons Microsatellite Repeats Point Mutation

Disciplines and Occupations2

Genetic Counseling Genetics, Medical

Anthropology, Education, Sociology and Social Phenomena1

Named Groups1

Health Care5

Family Health Genetic Testing Age of Onset Genetic Counseling Likelihood Functions

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 Named Groups Health Care

Penetrance Pedigree Genes, Dominant Heterozygote Mutation Phenotype Genetic Linkage Genetic Predisposition to Disease Optic Atrophy, Hereditary, Leber Lod Score Alleles Germ-Line Mutation Family Health Genotype DNA Mutational Analysis Genetic Testing Genes, BRCA1 Genes, Modifier Models, Genetic Age of Onset Founder Effect Hirschsprung Disease Chromosome Mapping Haplotypes Homozygote Genes, Recessive Jews Genetic Heterogeneity Gene Frequency Genetic Diseases, Inborn Genes, BRCA2 Dystonia Musculorum Deformans Mutation, Missense Family Syndrome Genetic Markers Heterozygote Detection Crosses, Genetic Dystonia BRCA2 Protein Amyloid Neuropathies, Familial Genetic Counseling Genetic Variation Angiomatosis Hemochromatosis Polymorphism, Single Nucleotide Syndactyly Abnormalities, Multiple Likelihood Functions Proto-Oncogene Proteins c-ret Craniofacial Abnormalities DNA, Mitochondrial Epistasis, Genetic Retinoblastoma Genetics, Medical Chromosomes, Human, Pair 19 RNA, Transfer, Ile Cardiomyopathy, Hypertrophic, Familial Bone Morphogenetic Protein Receptors, Type II Prealbumin Myoclonus Neoplastic Syndromes, Hereditary Inheritance Patterns Breast Neoplasms Mice, Transgenic Optic Atrophies, Hereditary Exons Dystonic Disorders Mice, Inbred C57BL Retinitis Pigmentosa Paraganglioma, Extra-Adrenal Microsatellite Repeats Point Mutation Genetic Association Studies Ovarian Neoplasms Eye Abnormalities

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