Human genomic imprinting. Medical search. Frequent questions

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Anatomy20

Endosperm Placenta Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 11 Germ Cells Chromosomes, Mammalian Embryo, Mammalian Blastocyst X Chromosome Zygote Seeds Hybrid Cells Cell Line Chromosomes, Artificial, Yeast Embryonic Stem Cells Chromosomes, Human, X Chromatin Chromosomes, Human Oocytes Spermatozoa

Organisms10

Platypus Marsupialia Macropodidae Mammals Hymenoptera Mice, Inbred C57BL Angiosperms Reptiles Chimera Mice, Transgenic

Diseases11

Beckwith-Wiedemann Syndrome Angelman Syndrome Prader-Willi Syndrome Uniparental Disomy Silver-Russell Syndrome Wilms Tumor Embryo Loss Genomic Instability Trophoblastic Tumor, Placental Site Genetic Diseases, Inborn Pseudohypoparathyroidism

Chemicals and Drugs30

RNA, Long Noncoding Insulin-Like Growth Factor II RNA, Untranslated Cyclin-Dependent Kinase Inhibitor p57 snRNP Core Proteins DNA DNA (Cytosine-5-)-Methyltransferase Receptor, IGF Type 2 GTP-Binding Protein alpha Subunits, Gs GRB10 Adaptor Protein RNA, Messenger DNA Primers Retroelements DNA Restriction Enzymes DNA, Complementary Proteins Genetic Markers Ribonucleoproteins, Small Nuclear Repressor Proteins Histones Sulfites Nuclear Proteins Transcription Factors DNA-Binding Proteins Chromatin DNA Modification Methylases KCNQ1 Potassium Channel DNA Probes DNA, Recombinant Muscle Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

Models, Genetic Chromosome Mapping Molecular Imprinting Cloning, Molecular Sequence Analysis, DNA Polymerase Chain Reaction Crosses, Genetic Nucleic Acid Hybridization Blotting, Southern Reproductive Techniques, Assisted Restriction Mapping Pedigree In Situ Hybridization, Fluorescence Cloning, Organism Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling Comparative Genomic Hybridization Oligonucleotide Array Sequence Analysis Sequence Alignment

Psychiatry and Psychology3

Imprinting (Psychology)Fathers Mothers

Phenomena and Processes73

Genomic Imprinting DNA Methylation Alleles Base Sequence Genome, Human Epigenesis, Genetic Uniparental Disomy Genomic Library Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 11 CpG Islands Genes Gene Expression Regulation, Developmental Parthenogenesis Exons Inheritance Patterns Genome Chromosomes, Mammalian Amino Acid Sequence Nucleic Acid Hybridization Biological Evolution Embryonic Development X Chromosome Inactivation Sequence Homology, Nucleic Acid Evolution, Molecular Placentation Promoter Regions, Genetic Gene Expression Regulation Introns Transcription, Genetic Gene Expression Pregnancy Quantitative Trait Loci Multigene Family Genetic Loci Genotype Genetic Linkage Mutation Phenotype Embryonic and Fetal Development Genomic Instability X Chromosome Genetic Variation Polymorphism, Single Nucleotide Polymorphism, Genetic Retroelements Gene Silencing Methylation Genetic Markers Dosage Compensation, Genetic Species Specificity Cosmids Repetitive Sequences, Nucleic Acid Organ Specificity Chromosomes, Artificial, Yeast Sex Characteristics Phylogeny Selection, Genetic Polymorphism, Restriction Fragment Length Pseudogenes Gene Dosage Sex Ratio Gene Deletion Chromosomes, Human, X Chromatin Chromosomes, Human Alu Elements Sequence Homology, Amino Acid Gene Library Heterozygote Long Interspersed Nucleotide Elements Genomic Islands Gene Expression Regulation, Plant

Disciplines and Occupations1

Anthropology, Education, Sociology and Social Phenomena3

Fathers Sex Ratio Mothers

Technology, Industry, Agriculture1

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Named Groups2

Fathers Mothers

Health Care1

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 Technology, Industry, Agriculture Information Science Named Groups Health Care

Genomic Imprinting RNA, Long Noncoding Beckwith-Wiedemann Syndrome DNA Methylation Insulin-Like Growth Factor II RNA, Untranslated Angelman Syndrome Prader-Willi Syndrome Alleles Base Sequence Molecular Sequence Data Cyclin-Dependent Kinase Inhibitor p57 Models, Genetic snRNP Core Proteins Endosperm Chromosome Mapping Genome, Human DNA Epigenesis, Genetic Uniparental Disomy Molecular Imprinting Cloning, Molecular Silver-Russell Syndrome Placenta Genomic Library Platypus Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 11 Sequence Analysis, DNA CpG Islands Imprinting (Psychology)DNA (Cytosine-5-)-Methyltransferase Genes Gene Expression Regulation, Developmental Parthenogenesis Exons Germ Cells Receptor, IGF Type 2 Polymerase Chain Reaction GTP-Binding Protein alpha Subunits, Gs Inheritance Patterns Genome Crosses, Genetic Chromosomes, Mammalian Marsupialia Amino Acid Sequence GRB10 Adaptor Protein Wilms Tumor Nucleic Acid Hybridization Biological Evolution Embryonic Development X Chromosome Inactivation Sequence Homology, Nucleic Acid Evolution, Molecular Placentation Fathers Promoter Regions, Genetic Embryo, Mammalian Blotting, Southern Gene Expression Regulation Introns RNA, Messenger Macropodidae Transcription, Genetic Gene Expression Genomics Pregnancy Reproductive Techniques, Assisted Quantitative Trait Loci Multigene Family DNA Primers Genetic Loci Genotype Embryo Loss Restriction Mapping Genetic Linkage Mutation Phenotype Embryonic and Fetal Development Blastocyst Genomic Instability X Chromosome Genetic Variation Pedigree Polymorphism, Single Nucleotide Polymorphism, Genetic In Situ Hybridization, Fluorescence Retroelements Gene Silencing Methylation DNA Restriction Enzymes DNA, Complementary Mammals Proteins Genetic Markers Dosage Compensation, Genetic Zygote Ribonucleoproteins, Small Nuclear Species Specificity Cosmids

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