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

Chemicals and Drugs9

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

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

Psychiatry and Psychology3

Laughter Intellectual Disability Fathers

Phenomena and Processes14

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

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 Werner Syndrome Uniparental Disomy RecQ Helicases Laughter Ribonucleoproteins, Small Nuclear Beckwith-Wiedemann Syndrome Chromosome Mapping Abnormalities, Multiple Chromosome Deletion Pedigree Phenotype Intellectual Disability Microcephaly Chromosome Inversion Mutation DNA Methylation In Situ Hybridization, Fluorescence Molecular Sequence Data Base Sequence Bardet-Biedl Syndrome Chromosome Breakage Microtubule Proteins Ataxia DNA Helicases Chromosome Banding Kallmann Syndrome Genetic Counseling Microsatellite Repeats Genetic Markers Sequence Deletion Mandibulofacial Dysostosis Autoantigens Methyl-CpG-Binding Protein 2 Fathers Polymerase Chain Reaction Chromosome Aberrations Smith-Lemli-Opitz Syndrome Peutz-Jeghers Syndrome

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