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Wessex Reg. Genetics CentreReset filters
88 results
  • Balanced translocation 45,XY,t(13;14)
  • Fragile X metaphase spread
  • Unbalanced translocation 46,XY,t(14;21)
  • Human metaphase, translocation, cosmid probe
  • Fragile X pedigree + rflp autoradiograph
  • Translocation shown using centromere probes
  • Genetics frame of reference - the size of various genetic components, including DNA, a base pair, various sizes of deletions, chromosomes and genes are listed and compared with more familiar objects such as the Solar System, planets, cities, hospitals, wards, and so on.
  • Turner's syndrome, centromere & cosmid probe
  • Whole arm translocation, centromere probes
  • Pericentric chromosome inversion
  • Duchenne muscular dystrophy control, FISH
  • Normal male 46,XY human karyotype
  • Prader Willi & Angelman's syndromes - probes
  • Interphase cells showing pentameric X
  • XYY syndrome karyotype 47,XYY
  • Aniridia + translocation, FISH & cosmid prob
  • Translocation shown up by cosmid probes
  • Unbalanced translocation 46,XY,t(13;14)
  • Inheritance of translocations
  • Foetal cells in amniotic fluid, + colchicine
  • Leukamia karyotype t(8;14)
  • Balanced translocation 46,XY,t(4;10)
  • Fragile X metaphase spread + nucleus
  • Chorionic villi explants in culture flask
  • XYY syndrome karyotype 46,XYY
  • Chronic myeloid leukaemia karyotype 9;22
  • Translocation - use of cosmid probe
  • Aniridia + deletion, FISH probes
  • Fragile X pedigree + rflp autoradiograph
  • Normal female 46,XX human karyotype