소장자료

Human Chromosome Variation: Heteromorphism and Polymorphism [electronic resource]

  • Wyandt, Herman E. author. , Tonk, Vijay S. author.
  • 2012
Human Chromosome Variation: Heteromorphism and Polymorphism [electronic resource]
  • 자료유형
    단행본
  • 서명/저자사항
    Human Chromosome Variation: Heteromorphism and Polymorphism[electronic resource] / by Herman E. Wyandt, Vijay S. Tonk.
  • 개인저자
    Wyandt, Herman E., author., Tonk, Vijay S., author.
  • 단체저자
    SpringerLink (Online service)
  • 형태사항
    XIX, 215 p. : online resource.
  • 내용주기
    Foreword -- Preface to Second Edition -- Acknowledgements -- List of Contributors -- A.혻 HUMAN CHROMOSOME METHODS AND NOMENCLATURE -- 1. Introduction -- 2.혻 Chromosome Heteromorphism -- 2.1혻 Chromosome Banding Techniques and Mechanisms -- 2.2 Other DNA-Binding Fluorochromes -- 2.3 Sister Chromatid Exchange Staining (SCE) -- 2.4 Replication Banding -- 2.5 High Resolution Banding and Special Treatments -- 2.6 Satellite DNA in Heteromorphic Regions -- 2.7 Single nucleotide polymorphisms (SNPs) -- 2.8 Fluorescence In Situ Hybridization (FISH) -- 3.혻 Frequencies Of Heteromorphisms -- 3.1 By Q- and C-banding -- 3.2혻 Specialized Banding Studies -- 4.혻 Clinical Populations -- 4.1 Spontaneous Abortions and Reproductive Failure -- 4.2혻 Non-disjunction -- 4.3혻 Satellite Association -- 4.4혻 Cancer -- 5. Euchromatic Variants -- B.혻 CHROMOSOME HETEROMORPHISM (SUMMARIES) -- Chromosome 1 -- Chromosome 2 -- Chromosome 3 -- Chromosome 4 -- Chromosome 5 -- Chromosome 6 -- Chromosome 7 -- Chromosome 8 -- Chromosome 9 -- Chromosome 10 -- Chromosome 11 -- Chromosome 12 -- Chromosome 13 -- Chromosome 14 -- Chromosome 15 -- Chromosome 16 -- Chromosome 17 -- Chromosome 18 -- Chromosome 19 -- Chromosome 20 -- Chromosome 21 -- Chromosome 22 -- Chromosome X -- Chromosome Y -- C. 혻Fish Variants -- 1.혻 FISH Results With Centromeric Repeats -- 2.혻 Subtelomeric Deletions/Duplications: Normal Variation or Chromosome Abnormality -- D. Fragile Sites -- E. Comparative Genomic Hybridization-Microarray Analysis, Copy Number Variants, and Clinical Interpretation -- 1.혻 Introduction -- 2. Case Discussions -- 2.1 Cases where the interpretation of clinical significance is clear and the diagnosis provides good혻 prognostic information -- 2.2 Cases where interpretation of clinical significance is clear but the finding gives less defined prognosis -- 2.3 Cases of familial change with unclear significance or prognosis -- 3. Summary -- Index 혻.
  • 일반주제명
    Medicine.
    Human genetics.
    Medical genetics.
    Cytogenetics.
    Microarrays.
    Biotechnology.
    Biomedicine.
    Cytogenetics.
    Human Genetics.
    Gene Function.
    Microarrays.
    Biotechnology.
  • 기본자료 저록
    Springer eBooks
  • 기타형태 저록
    Printed edition: 9789400708952
  • ISBN
    9789400708969
  • 언어
    영어