Paternal angelman syndrome gene. Medical search. Frequent questions

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Anatomy1

Chromosomes, Human, Pair 15

Diseases19

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 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 Autoantigens Methyl-CpG-Binding Protein 2 Genetic Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment4

Chromosome Mapping Pedigree In Situ Hybridization, Fluorescence Chromosome Banding

Psychiatry and Psychology3

Laughter Intellectual Disability Fathers

Phenomena and Processes13

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

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 Abnormalities, Multiple Chromosome Mapping Chromosome Deletion Pedigree Intellectual Disability Microcephaly Chromosome Inversion Phenotype DNA Methylation Bardet-Biedl Syndrome Mutation In Situ Hybridization, Fluorescence Chromosome Breakage Microtubule Proteins Ataxia DNA Helicases Kallmann Syndrome Genetic Counseling Mandibulofacial Dysostosis Chromosome Banding Autoantigens Methyl-CpG-Binding Protein 2 Sequence Deletion Microsatellite Repeats Fathers Genetic Markers Molecular Sequence Data Smith-Lemli-Opitz Syndrome Base Sequence Peutz-Jeghers Syndrome

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