Deletion angelman syndrome gene. Medical search. Frequent questions

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Anatomy1

Chromosomes, Human, Pair 15

Diseases20

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

Chemicals and Drugs9

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

Chromosome Mapping Pedigree In Situ Hybridization, Fluorescence Chromosome Banding Polymerase Chain Reaction Disease Models, Animal

Psychiatry and Psychology3

Laughter Intellectual Disability Fathers

Phenomena and Processes15

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

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science2

Molecular Sequence Data Base Sequence

Named Groups1

Health Care1

Genetic Counseling

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

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