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94 results
  • Turner's syndrome, centromere & cosmid probe
  • Chronic myeloid leukaemia karyotype 9;22
  • Fragile X diagnostic test - male, no stain
  • Follicular non-Hodgkinson's lymphoma
  • Acute myeloblastic leukaemia karyotype
  • Leukaemia karyotype t(4;11) etc
  • Fragile X diagnostic test - normal
  • Fragile X diagnostic test - male, no stain
  • Pressure Palsy, deletion c'some 17, cosmid
  • Turner's stndrome, centromere & cosmid probe
  • Unbalanced translocation, cosmid probe
  • Pressure palsy, deletion c'some 17, cosmid
  • Klinefelter's syndrome karyotype 47,XXY
  • Duchenne muscular dystrophy pedigree + rflp
  • Unbalanced translocation 46,XY,t(14;21)
  • Pericentric chromosome inversion
  • Unbalanced translocation 46,XY,t(13;14)
  • Balanced translocation 46,XY,t(4;10)
  • Fragile X diagnostic test - female carrier
  • Paracentric chromosome inversion
  • Prader Willi & Angelman syndromes - FISH
  • Translocation shown up by cosmid probe
  • 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
  • Balanced translocation 45,XY,t(14;21)
  • Unbalanced translocation 46,XY,t(21;21)
  • Huntington's chorea pedigree, constructed from
  • Patau's syndrome karyotype 47,XY,+13
  • Balanced translocation 45,XY,t(21;21)
  • Meeting the challenge of disabling disease : animal research brings hope / Research for Health Charities Group.
  • Diagnostic test for Fragile X, using presence (normal) or absence (Fragile X syndrome) of FMR-1 protein. FMR-1 protein expression in blood cells has been made visible with antibodies against the FMR-1 protein. The presence of FMR-1 protein is made visible as red staining. a: red staining in cells of normal individual. b/c: absence of staining in male patient. d: female patient; one cell is showing staining and in the other cell there is an absence of staining - this individual is a carrier.