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Chromosomes X Chromosome Sex Chromosomes Chromosomes, Human, Pair 1 Chromosomes, Human Chromosomes, Bacterial Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 21 Chromosomes, Plant Chromosomes, Fungal Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 22 Chromosomes, Mammalian Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 10 Chromosomes, Human, Y Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 19 Chromosomes, Artificial, Bacterial Chromosomes, Human, X Chromosomes, Human, 1-3 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 18 Chromosomes, Human, 16-18 Chromosomes, Human, Pair 20 Chromosomes, Artificial, Yeast Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Ring Chromosomes Chromosomes, Human, 4-5 Centromere Chromosomes, Insect Hybrid Cells Chromosome Structures Chromosomes, Human, 19-20 Chromosomes, Artificial, Human Kinetochores Telomere Spindle Apparatus Chromatids Polytene Chromosomes Chromatin Spermatocytes Philadelphia Chromosome Cell Line Chromosomes, Archaeal Cell Nucleus Sex Chromatin Chromosomes, Artificial Microtubules Euchromatin Spermatozoa HeLa Cells Chromosomes, Artificial, P1 Bacteriophage Lymphocytes Oocytes

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Drosophila melanogaster Saccharomyces cerevisiae Escherichia coli Drosophila Triticum Animals, Congenic Cricetinae Secale cereale Muridae Schizosaccharomyces Mice, Inbred Strains Platypus

Diseases29

Chromosome Aberrations Chromosome Deletion Chromosome Disorders Chromosome Breakage Ring Chromosomes Chromosome Inversion Translocation, Genetic Aneuploidy Trisomy Nondisjunction, Genetic Chromosomal Instability Chromosome Fragility Chromosome Duplication Abnormalities, Multiple Polyploidy Sex Chromosome Disorders Monosomy Genetic Predisposition to Disease Philadelphia Chromosome Intellectual Disability Syndrome Down Syndrome Sex Chromosome Disorders of Sex Development Uniparental Disomy Turner Syndrome Infertility, Male Klinefelter Syndrome Prader-Willi Syndrome Genomic Instability

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Genetic Markers DNA Chromosomal Proteins, Non-Histone DNA, Satellite DNA Probes Cell Cycle Proteins DNA-Binding Proteins Nuclear Proteins Chromatin DNA, Bacterial DNA Transposable Elements Azure Stains DNA Primers DNA, Neoplasm Histones DNA, Fungal Euchromatin DNA, Plant Aurora Kinases DNA, Complementary DNA Restriction Enzymes Transcription Factors Saccharomyces cerevisiae Proteins Bacterial Proteins Drosophila Proteins RNA, Messenger Protein-Serine-Threonine Kinases Aurora Kinase B

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

Chromosome Mapping Chromosome Banding Chromosome Painting Karyotyping In Situ Hybridization, Fluorescence Pedigree Crosses, Genetic Cloning, Molecular Nucleic Acid Hybridization Chromosome Walking Blotting, Southern Models, Genetic Sequence Analysis, DNA Polymerase Chain Reaction Cytogenetic Analysis Contig Mapping Hybridization, Genetic Sequence Alignment Radiation Hybrid Mapping Comparative Genomic Hybridization DNA Mutational Analysis Genetic Complementation Test Microscopy, Fluorescence Sex Determination Analysis Mutagenesis, Insertional Genome-Wide Association Study

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes170

Chromosomes X Chromosome Chromosome Aberrations Sex Chromosomes Chromosomes, Human, Pair 1 Chromosomes, Human Chromosomes, Bacterial Chromosome Segregation Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 6 Chromosome Deletion Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 21 Chromosomes, Plant Chromosomes, Fungal Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 22 Chromosome Pairing Chromosomes, Mammalian Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 10 Chromosomes, Human, Y Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 19 Chromosomes, Artificial, Bacterial Chromosomes, Human, X Chromosomes, Human, 1-3 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 18 Chromosomes, Human, 16-18 Chromosomes, Human, Pair 20 Chromosomes, Artificial, Yeast Chromosomes, Human, 13-15 Genetic Linkage Chromosome Breakage Chromosomes, Human, 21-22 and Y Ring Chromosomes Chromosome Inversion Genetic Markers Chromosome Positioning Chromosomes, Human, 4-5 X Chromosome Inactivation Centromere Base Sequence Chromosomes, Insect Translocation, Genetic Meiosis Chromosome Structures Chromosomes, Human, 19-20 Aneuploidy Metaphase Mitosis Recombination, Genetic Lod Score Mutation Microsatellite Repeats Phenotype Alleles Trisomy Nondisjunction, Genetic Chromosomes, Artificial, Human Kinetochores Nucleic Acid Hybridization Telomere Amino Acid Sequence Chromosomal Instability Chromosome Fragility Genotype Quantitative Trait Loci Haplotypes Chromosome Duplication DNA, Satellite Genes Repetitive Sequences, Nucleic Acid Diploidy Evolution, Molecular Chromatids Mosaicism Heterozygote Polytene Chromosomes Multigene Family Polyploidy DNA Replication Gene Deletion Prophase Interphase Gene Dosage Loss of Heterozygosity Genome, Human Genetic Variation Karyotype Polymorphism, Genetic Cosmids Chromosome Fragile Sites Gene Rearrangement Chromatin Monosomy Plasmids Genes, X-Linked Sequence Tagged Sites Polymorphism, Restriction Fragment Length Genes, Dominant Species Specificity Polymorphism, Single Nucleotide DNA Transposable Elements Genetic Predisposition to Disease Philadelphia Chromosome Genes, Recessive Chromosomes, Archaeal Sequence Homology, Nucleic Acid Chromosome Breakpoints Genome Ploidies Homozygote Haploidy Phylogeny Sequence Homology, Amino Acid Genetic Loci Sex Chromatin Genomic Imprinting Gene Duplication Hybridization, Genetic Gene Amplification Genes, Lethal Transcription, Genetic Genes, Bacterial Genome, Plant Chromosomes, Artificial Sister Chromatid Exchange Pachytene Stage Exons Genes, Y-Linked Euchromatin Genes, Tumor Suppressor Sex Determination Processes Genes, Insect Meiotic Prophase I Quantitative Trait, Heritable Gene Library Genetic Heterogeneity Linkage Disequilibrium Genomic Library Cell Cycle Uniparental Disomy Sequence Deletion Biological Evolution Chromosomes, Artificial, P1 Bacteriophage Introns Pseudogenes Genes, Fungal Genes, Plant Gene Order Consanguinity Gene Frequency Replication Origin Gene Expression Regulation Gene Expression Mutagenesis, Insertional Spermatogenesis Genome, Bacterial Open Reading Frames Genomic Instability

Disciplines and Occupations1

Technology, Industry, Agriculture2

Triticum Secale cereale

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny

Health Care1

Genome-Wide Association Study

MOLECULAR MAPPING OF THE 7Q-DELETION IN MYELOID DISORDERS - Radcliffe Department of Medicine

We use cookies to ensure that we give you the best experience on our website. If you click Continue well assume that you are happy to receive all cookies and you wont see this message again. Click Find out more for information on how to change your cookie settings ...

https://www.rdm.ox.ac.uk/publications/375568

Genomic profiling of AML and MDS yields prognostic clues | MDedge Hematology and Oncology

Orlando - A genome-wide study of blood and bone marrow samples from more than 1,300 adults with myeloid disorders has both confirmed the role of known or suspec

https://www.mdedge.com/hematology-oncology/article/215282/aml/genomic-profiling-aml-and-mds-yields-prognostic-clues

Michelle M. LeBeau, Ph.D - Cancer Research Foundation

Associate Professor, Section of Hematology/Oncology, Co-Director, Hematology/Oncology Cytogenetics Laboratory , University of Chicago. Molecular-Cytogenetic Analysis of the Deletions of Chromosomes 5 and 7 in Malignant Myeloid Disorders. ...

https://www.cancerresearchfdn.org/recipient/michelle-m-lebeau/?back=fletcher-scholars-program

Malignant characteristics of somatic cell hybrids of normal human and by M R. Bordelon

Bordelon, M R., Malignant characteristics of somatic cell hybrids of normal human and malignant mouse cells. Abstr. (1974). Subject Strain Bibliography 1974. 446 ...

https://mouseion.jax.org/ssbb1974/446/

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