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229 results
  • Fragile X metaphase spread + nucleus
  • Fragile X metaphase spread + nucleus
  • Fragile X metaphase spread
  • Down's syndrome karyotype 47,XX,+21
  • DiGeorge syndrome - 22q11deletion - FISH
  • Balanced translocation 45,XY,t(21;21)
  • Down syndrome human karyotype 47,XY,+21
  • Inheritance of translocations
  • Huntington's chorea pedigree, constructed from
  • Movie: 16 dpc mouse heart
  • DNA probe for human/hamster hybrid DNA
  • Drosophila development, calcium & histones
  • Translocation - use of cosmid probe
  • XYY syndrome karyotype 47,XYY
  • Human metaphase, normal male + nucleus
  • Drosophila development, calcium/histones, movie
  • XYY syndrome karyotype 46,XYY
  • Leukaemia karyotype t(4;11) etc
  • Human metaphase, translocation, cosmid probe
  • Aniridia, Wilm's tumour, deletion - FISH
  • Use of DNA probe on c-some 9 heterochromatin
  • Fragile X pedigree + rflp autoradiograph
  • Unbalanced translocation, cosmid probe
  • Myelodysplasia (leukaemia) karyotype
  • Turner's stndrome, centromere & cosmid probe
  • Duchenne muscular dystrophy pedigree + rflp
  • Chronic myeloid leukaemia karyotype 9;22
  • Aniridia + deletion, FISH probes
  • DiGeorge syndrome - deleted/nondeleted FISH
  • Leukaemia karyotype, acute myelodysplasia