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94 results
  • Fragile X metaphase spread + nucleus
  • Fragile X metaphase spread + nucleus
  • Fragile X metaphase spread
  • Interphase cells showing pentameric X
  • XYY syndrome karyotype 47,XYY
  • Translocation shown up by cosmid probes
  • Translocation, shown by cosmid probes
  • DiGeorge syndrome - deleted/nondeleted FISH
  • Human metaphase, translocation, cosmid probe
  • Aniridia + translocation, FISH & cosmid prob
  • Leukamia karyotype t(8;14)
  • XYY syndrome karyotype 46,XYY
  • Metaphase, deletion on chromosome 15
  • Familial aniridia deletion shown by cosmid
  • Turner's syndrome karyotype 45,XO. This female lacks the second X chromosome present in the normal karyotype. Symptoms include short stature, neck wbbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The ovaries are reduced to fibrous streaks. Also known as XO syndrome or ovarian short-stature syndrome.
  • Down syndrome human karyotype 47,XY,+21
  • Triple-X chromosome aberration karyotype
  • Duchenne muscular dystrophy pedigree chart
  • Fragile X chromosome, atomic force microscope
  • Translocation shown using centromere probes
  • Whole arm translocation, centromere probes
  • Aniridia + deletion, FISH probes
  • 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