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  • Turner's stndrome, centromere & cosmid probe

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • XYY syndrome karyotype 47,XYY

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Normal human male metaphase, Y banding

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Inversion in X chromosome

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Duchenne muscular dystrophy pedigree chart

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Acute myelomonocytic leukaemia +eosinophilia

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Fragile X pedigree + rflp autoradiograph

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Pressure palsy, deletion c'some 17, cosmid

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Paracentric chromosome inversion

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Foetal cells in amniotic fluid, low power LM

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Foetal cells from amniotic fluid in culture

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Translocation shown using centromere probes

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Fragile X pedigree + rflp autoradiograph

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Down syndrome human karyotype 47,XY,+21

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Familial aniridia deletion shown by cosmid

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Prader Willi & Angelman's syndromes - probes

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Duchenne muscular dystrophy deletion, FISH

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Translocation - use of cosmid probe

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Edward's syndrome karyotype, 47,XY,+18

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Klinefelter's syndrome karyotype 47,XXY

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Interphase cells showing pentameric X

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Balanced reciprocal translocation 46,XY,t(2;5). This male has a chromosomal disorder. A chromosome 2 and a chromosome 5 have exchanged segments. The cell still contains a complete complement of

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Balanced translocation 45,XY,t(21;21)

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Foetal cells from amniotic fluid, colchicine

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online

  • Down's syndrome karyotype 47,XX,+21

    • Wessex Reg. Genetics Centre
    • Digital Images
    • Online
88 results
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