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Wessex Reg. Genetics CentreReset filters
88 results
  • Fragile X metaphase spread + nucleus
  • Balanced translocation 45,XY,t(14;21)
  • Leukaemia karyotype, acute myelodysplasia
  • Foetal cells in amniotic fluid, low power LM
  • Foetal cells from amniotic fluid in culture
  • Chromosome condensation prophase to metaphas
  • Pressure Palsy, deletion c'some 17, cosmid
  • Duchenne muscular dystrophy carrier female
  • DiGeorge syndrome - deleted/nondeleted FISH
  • Down's syndrome karyotype 47,XX,+21
  • Turner's stndrome, centromere & cosmid probe
  • Unbalanced translocation 46,XY,t(21;21)
  • Klinefelter's syndrome karyotype 47,XXY
  • Foetal cells from amniotic fluid in culture
  • Huntington's chorea pedigree, constructed from
  • Triple-X chromosome aberration karyotype
  • Unbalanced translocation, cosmid probe
  • Pressure palsy, deletion c'some 17, cosmid
  • Duchenne muscular dystrophy pedigree chart
  • Prader Willi & Angelman's syndromes - probes
  • Patau's syndrome karyotype 47,XY,+13
  • Chorionic villi samples in petri dish
  • Normal male 46,XY human karyotype
  • Inversion in X chromosome
  • Balanced translocation 45,XY,t(21;21)
  • Klinefelter's syndrome karyotype 47,XXY
  • Hyperdiploid acute lymphoblastic leukaemia
  • Duchenne muscular dystrophy pedigree + rflp