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295 results
  • Fragile X pedigree + rflp autoradiograph
  • DiGeorge syndrome - 22q11deletion - FISH
  • Myelodysplasia (leukaemia) karyotype
  • Triple-X chromosome aberration karyotype
  • Aniridia, Wilm's tumour, deletion - FISH
  • Leukaemia karyotype, acute myelodysplasia
  • Klinefelter's syndrome karyotype 47,XXY
  • Inversion in X chromosome
  • Turner's syndrome, centromere & cosmid probe
  • Chronic myeloid leukaemia karyotype 9;22
  • Follicular non-Hodgkinson's lymphoma
  • Acute myeloblastic leukaemia karyotype
  • Leukaemia karyotype t(4;11) etc
  • Pressure Palsy, deletion c'some 17, cosmid
  • Turner's stndrome, centromere & cosmid probe
  • Unbalanced translocation, cosmid probe
  • Pressure palsy, deletion c'some 17, cosmid
  • Klinefelter's syndrome karyotype 47,XXY
  • Duchenne muscular dystrophy pedigree + rflp
  • Pericentric chromosome inversion
  • Paracentric chromosome inversion
  • Prader Willi & Angelman syndromes - FISH
  • Translocation shown up by cosmid probe
  • Huntington's chorea pedigree, constructed from
  • Patau's syndrome karyotype 47,XY,+13
  • Duchenne muscular dystrophy control, FISH
  • Fragile X metaphase spread
  • Duchenne muscular dystrophy deletion, FISH
  • Down syndrome human karyotype 47,XY,+21
  • Foetal cells from amniotic fluid, colchicine