Autosomal dominant inheritance pattern. Medical search. Frequent questions

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Anatomy5

Ultimobranchial Body Toes Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 12 X Chromosome

Diseases15

Hand Deformities, Congenital Dystonia Musculorum Deformans Syndrome Foot Deformities, Congenital Hypertelorism Abnormalities, Multiple Syndactyly Chromosome Disorders Genetic Predisposition to Disease Polycystic Kidney, Autosomal Dominant Retinitis Pigmentosa Myotonia Congenita Chromosome Aberrations Muscle Cramp Cleft Lip

Chemicals and Drugs4

Genetic Markers TRPP Cation Channels DNA, Mitochondrial DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

Pedigree Chromosome Mapping DNA Mutational Analysis Crosses, Genetic Models, Genetic Polymerase Chain Reaction Sequence Analysis, DNA Genetic Testing

Psychiatry and Psychology1

Phenomena and Processes27

Genes, Dominant Inheritance Patterns Genetic Linkage Lod Score Genes, Recessive Mutation Penetrance Phenotype Heterozygote Genetic Predisposition to Disease Genetic Markers Haplotypes Genetic Heterogeneity Mutation, Missense Genotype Microsatellite Repeats Chromosomes, Human, Pair 16 Alleles Base Sequence Consanguinity Chromosome Aberrations Point Mutation Polymorphism, Genetic Chromosomes, Human, Pair 12 Exons Homozygote X Chromosome

Anthropology, Education, Sociology and Social Phenomena1

Information Science2

Molecular Sequence Data Base Sequence

Health Care3

Family Health Age of Onset Genetic Testing

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Health Care

Pedigree Genes, Dominant Inheritance Patterns Genetic Linkage Lod Score Genes, Recessive Hand Deformities, Congenital Family Health Dystonia Musculorum Deformans Syndrome Foot Deformities, Congenital Ultimobranchial Body Chromosome Mapping Hypertelorism Mutation Abnormalities, Multiple Syndactyly Penetrance Phenotype Chromosome Disorders Toes Heterozygote DNA Mutational Analysis Age of Onset Genetic Predisposition to Disease Genetic Markers Haplotypes Genetic Heterogeneity Mutation, Missense Polycystic Kidney, Autosomal Dominant Genotype Microsatellite Repeats Chromosomes, Human, Pair 16 Crosses, Genetic Molecular Sequence Data Family Retinitis Pigmentosa Alleles Models, Genetic Base Sequence Polymerase Chain Reaction Consanguinity Myotonia Congenita Chromosome Aberrations Muscle Cramp Point Mutation Polymorphism, Genetic Cleft Lip Sequence Analysis, DNA Genetic Testing TRPP Cation Channels Chromosomes, Human, Pair 12 DNA, Mitochondrial Exons Homozygote X Chromosome DNA

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