Uniparental angelman syndrome gene. Medical search. Frequent questions

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Anatomy1

Chromosomes, Human, Pair 15

Organisms1

Diseases21

Angelman Syndrome Uniparental Disomy Prader-Willi Syndrome Syndrome Bloom Syndrome Beckwith-Wiedemann Syndrome Werner Syndrome Abnormalities, Multiple Chromosome Deletion Intellectual Disability Chromosome Inversion Microcephaly Chromosome Aberrations Bardet-Biedl Syndrome Chromosome Breakage Dwarfism Ataxia Kallmann Syndrome Mandibulofacial Dysostosis Smith-Lemli-Opitz Syndrome Peutz-Jeghers Syndrome

Chemicals and Drugs9

snRNP Core Proteins Ubiquitin-Protein Ligases RecQ Helicases Ribonucleoproteins, Small Nuclear Genetic Markers Microtubule Proteins Autoantigens DNA Helicases Methyl-CpG-Binding Protein 2

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

Pedigree Chromosome Mapping In Situ Hybridization, Fluorescence Karyotyping Chromosome Banding Blotting, Southern Polymerase Chain Reaction

Psychiatry and Psychology3

Laughter Fathers Intellectual Disability

Phenomena and Processes18

Uniparental Disomy Chromosomes, Human, Pair 15 Genomic Imprinting Chromosome Deletion Phenotype Chromosome Inversion DNA Methylation Mutation Chromosome Aberrations Microsatellite Repeats Mosaicism Genetic Markers Chromosome Breakage Homozygote Base Sequence Alleles Sequence Deletion Genotype

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science2

Base Sequence Molecular Sequence Data

Named Groups1

Health Care1

Genetic Counseling

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

Angelman Syndrome Uniparental Disomy Prader-Willi Syndrome Chromosomes, Human, Pair 15 Genomic Imprinting snRNP Core Proteins Syndrome Ubiquitin-Protein Ligases Bloom Syndrome Beckwith-Wiedemann Syndrome Werner Syndrome RecQ Helicases Abnormalities, Multiple Ribonucleoproteins, Small Nuclear Laughter Pedigree Chromosome Deletion Chromosome Mapping Fathers Phenotype Intellectual Disability Chromosome Inversion DNA Methylation In Situ Hybridization, Fluorescence Mutation Microcephaly Chromosome Aberrations Microsatellite Repeats Karyotyping Mosaicism Bardet-Biedl Syndrome Chromosome Banding Genetic Markers Chromosome Breakage Dwarfism Microtubule Proteins Ataxia Autoantigens DNA Helicases Homozygote Base Sequence Molecular Sequence Data Kallmann Syndrome Genetic Counseling Mandibulofacial Dysostosis Alleles Methyl-CpG-Binding Protein 2 Sequence Deletion Bivalvia Genotype Blotting, Southern Smith-Lemli-Opitz Syndrome Peutz-Jeghers Syndrome Polymerase Chain Reaction

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