Wellcome uses cookies.

Read our policy
Skip to main content
35 results filtered with: Karyotype
  • Balanced translocation 45,XY,t(13;14)
  • Unbalanced translocation 46,XY,t(14;21)
  • Pericentric chromosome inversion
  • Unbalanced translocation 46,XY,t(13;14)
  • Inheritance of translocations
  • Leukamia karyotype t(8;14)
  • Balanced translocation 46,XY,t(4;10)
  • XYY syndrome karyotype 46,XYY
  • Chronic myeloid leukaemia karyotype 9;22
  • Fragile X metaphase spread
  • Acute promyelocytic leukaemia karyotype
  • Paracentric chromosome inversion
  • 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
  • Myelodysplasia (leukaemia) karyotype
  • Follicular non-Hodgkinson's lymphoma
  • Acute myelomonocytic leukaemia +eosinophilia
  • Triple-X chromosome aberration karyotype
  • Balanced reciprocal translocation 46,XY,t(2;5). This male has a chromosomal disorder. A chromosome 2 and a chromosome 5 have exchanged segments. The cell still contains a complete complement of
  • Normal female 46,XX human karyotype
  • Acute myeloblastic leukaemia karyotype
  • 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.
  • Edward's syndrome karyotype, 47,XY,+18
  • Leukaemia karyotype t(4;11) etc
  • Balanced translocation 45,XY,t(14;21)
  • Leukaemia karyotype, acute myelodysplasia
  • Chromosome condensation prophase to metaphas
  • Down's syndrome karyotype 47,XX,+21
  • Unbalanced translocation 46,XY,t(21;21)
  • Patau's syndrome karyotype 47,XY,+13