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43 results
  • Myelodysplasia (leukaemia) karyotype
  • Acute myeloblastic leukaemia karyotype
  • Acute promyelocytic leukaemia karyotype
  • Leukaemia karyotype, acute myelodysplasia
  • XYY syndrome karyotype 47,XYY
  • XYY syndrome karyotype 46,XYY
  • Triple-X chromosome aberration karyotype
  • Triple-X chromosome aberration karyotype
  • Leukamia karyotype t(8;14)
  • Klinefelter's syndrome karyotype 47,XXY
  • Klinefelter's syndrome karyotype 47,XXY
  • Down's syndrome karyotype 47,XX,+21
  • Leukaemia karyotype t(4;11) etc
  • Chronic myeloid leukaemia karyotype 9;22
  • Edward's syndrome karyotype, 47,XY,+18
  • Normal female 46,XX human karyotype
  • Normal male 46,XY human karyotype
  • Normal female 46,XX human karyotype
  • Normal male 46,XY human karyotype
  • Patau's syndrome karyotype 47,XY,+13
  • Down syndrome human karyotype 47,XY,+21
  • Down syndrome human karyotype 47,XY,+21
  • 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.
  • Human karyotype showing translocation between chromosomes 14 and 21, t(14;21). This is a balanced translocation - the cell retains a normal complement of genetic information.
  • Follicular non-Hodgkinson's lymphoma
  • Hyperdiploid acute lymphoblastic leukaemia
  • Acute myelomonocytic leukaemia +eosinophilia
  • Chromosome condensation prophase to metaphas
  • Inheritance of translocations
  • Balanced translocation 45,XY,t(13;14)