Wellcome uses cookies.

Read our policy
Wellcome Collection homepage
All
Stories
Images
Catalogue
Events

Active filters:

GENETIC DISEASEReset filters
42 results
  • Fragile X metaphase spread
  • Human metaphase, translocation, cosmid probe
  • Translocation shown using centromere probes
  • Turner's syndrome, centromere & cosmid probe
  • Whole arm translocation, centromere probes
  • Duchenne muscular dystrophy control, FISH
  • Prader Willi & Angelman's syndromes - probes
  • XYY syndrome karyotype 47,XYY
  • Aniridia + translocation, FISH & cosmid prob
  • Translocation shown up by cosmid probes
  • Leukamia karyotype t(8;14)
  • Fragile X metaphase spread + nucleus
  • Fragile X diagnostic test - female carrier
  • Chronic myeloid leukaemia karyotype 9;22
  • Aniridia + deletion, FISH probes
  • Fragile X pedigree + rflp autoradiograph
  • DiGeorge syndrome - 22q11deletion - FISH
  • Familial aniridia deletion shown by cosmid
  • Duchenne muscular dystrophy deletion, FISH
  • Prader Willi & Angelman syndromes - FISH
  • Translocation, shown by cosmid probes
  • Fragile X diagnostic test - male, no stain
  • Myelodysplasia (leukaemia) karyotype
  • Down syndrome human karyotype 47,XY,+21
  • Translocation shown up by cosmid probe
  • Aniridia, Wilm's tumour, deletion - FISH
  • Acute myeloblastic leukaemia karyotype
  • Fragile X metaphase spread + nucleus
  • Fragile X diagnostic test - normal
  • Fragile X diagnostic test - male, no stain