eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

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  1. Biochemistry
  2. Bioethics & Philosophy
  3. Cell Biology
  4. Developmental Biology
  5. Ecology
  6. Evolution & Diversity of Life
  7. Genetics & Disease
    1. Bioinformatics and Genetic Disease
    2. Cancer Genetics
    3. Chromosomal Disorders
    4. Epigenetics and Disease
    5. Forensic Genetics
    6. Gene and Genome Structure and Organisation
    7. Gene Expression Profiling of Genetic Disease
    8. Gene Mapping by Disease Association
    9. Gene Therapy
    10. General Genetics and Disease
    11. Genetic Counseling
    12. Genetic Models
    13. Genetics of Intelligence and Cognition
    14. Genomic Disorders
      1. Ageing Genes: Gerontogenes
      2. Anticipation
      3. Autism Spectrum Disorders: Genes and Genomic Mechanisms
      4. Biallelic Germline Mutations of Mismatch-Repair Genes and Paediatric Malignancies
      5. Cancer: Chromosomal Abnormalities
      6. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      7. Chromatin Structure and Modification: Defects
      8. Chromosomal Genetic Disease: Structural Aberrations
      9. Chromosomal Instability (CIN) in Cancer
      10. Chromosomal Numerical Aberrations
      11. Chromosome 10
      12. Chromosome 15
      13. Chromosome Instability (CIN), Aneuploidy and Cancer
      14. Chromothripsis and Human Genetic Disease
      15. Cis-Regulatory Mutations in Human Disease
      16. Comparative Genomic Hybridization in the Study of Human Disease
      17. Copy Number Variations and Neuropsychiatric Diseases
      18. DNA Repair Disorders
      19. Down Syndrome
      20. Expanding Mutations/Genetic Anticipation
      21. Fragile Sites and Human Disease
      22. Fusion Proteins and Diseases
      23. Gene Conversion in Evolution and Disease
      24. Genetic Imprinting in the Prader–Willi and Angelman Syndromes
      25. Genetics of Chromosome 22q11.2 Deletion Syndrome
      26. Genetics of Silver–Russell Syndrome
      27. Genomic and Chromosomal Instability
      28. Genomic Arrays in Prenatal Diagnosis
      29. Genomic Imprinting at the Transcriptional Level
      30. Genomic Rearrangements: Mutational Mechanisms
      31. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      32. Hepatocellular Carcinoma
      33. Human Embryonic Aneuploidy
      34. Imprinting (Mammals)
      35. Infertility: Genetic Disorders
      36. Intellectual Disability: Genetics
      37. Mechanisms of Chromosome Translocations in Cancer
      38. Mechanisms of RNA-Induced Toxicity in Diseases Characterised by CAG Repeat Expansions
      39. Microdeletion Syndromes
      40. Microdeletions and Microduplications: Mechanism
      41. MicroRNAs and Human Disease
      42. Microsatellite Instability
      43. Mitochondrial Heteroplasmy and Disease
      44. Mitosis: Chromosome Segregation and Stability
      45. Molecular Genetic Causes of Discordance in Monozygotic Twins
      46. Molecular Genetics of Incontinentia Pigmenti
      47. Molecular Genetics of Mental Retardation
      48. Molecular Genetics of Myelodysplastic Syndromes
      49. Molecular Genetics of Rhabdomyosarcoma
      50. Molecular Genetics of Spermatogenic Disturbances
      51. The Molecular Genetics of Trisomy 18: Phenotype–Genotype Correlations
      52. Molecular Genetics of Williams–Beuren Syndrome
      53. Molecular Mechanisms Underlying Pathogenic Missense Mutations
      54. You have free access to this content
        Monosomies
      55. Mosaicism
      56. Non-B DNA Structure and Mutations Causing Human Genetic Disease
      57. Noncoding RNAs in Biology and Disease
      58. Origins of Human Aneuploidy
      59. Pathogenic Mechanisms and Clinical Consequences of Chromosomal Aberrations in Man
      60. Polyploidy
      61. Pseudoautosomal Inheritance
      62. Relevance of Copy Number Variation to Human Genetic Disease
      63. Repetitive Elements and Human Disorders
      64. Retrotransposons and Human Disease
      65. Role of Endogenous Retroviruses in Human Genetic Diseases
      66. Schizophrenia and 22q11.2 Deletion Syndrome
      67. Segmental Duplications and Genetic Disease
      68. Segmental Duplications: A Source of Diversity, Evolution and Disease
      69. Sex Chromosome Abnormalities
      70. Somatic Genome Variations
      71. Sotos Syndrome
      72. Spontaneous Function Correction of Pathogenic Alleles in Inherited Diseases Resulting in Somatic Mosaicism
      73. SRY, Sex Determination and Gonadal Differentiation
      74. Studying Genomic and Epigenetic Aberrations by Microarray Profiling
      75. Tandem Repeat Instability and Genome Evolution
      76. Translocation Breakpoints in Cancer
      77. Transposons as Natural and Experimental Mutagens
      78. You have free access to this content
        Trisomy
      79. Uniparental Disomy
      80. Uniparental Disomy in Cancer – A New Tool in Molecular Cancer
      81. X-Chromosome Inactivation
      82. X-chromosome Inactivation and Disease
      83. XYY Syndrome
      84. Y-chromosome-linked Traits
    15. Inter-Individual Variation and Polymorphism
    16. Linkage Analysis
    17. Mitochondrial Diseases
    18. Model Organisms and Human Disease
    19. Molecular Genetics of Common and Complex Disease
    20. Mutational Mechanisms of Genetic Disease
    21. Pharmacogenetics and Pharmacogenomics
    22. Proteomic Studies of Genetic Disease
    23. Quantitative Genetics
    24. Specific Genetic Disorders
    25. Statistical Methodology in Genetics
    26. Techniques and Tools in Clinical Genetics
  8. Immunology
  9. Microbiology
  10. Molecular Biology
  11. Neuroscience
  12. Plant Science
  13. Science & Society
  14. Structural Biology
  15. Virology

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