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Genetic Diseases, InbornReset filters
87 results
  • Fragile X metaphase spread
  • Unbalanced translocation 46,XY,t(14;21)
  • Fragile X chromosome, atomic force microscope
  • 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.
  • Human metaphase, translocation, cosmid probe
  • Translocation shown using centromere probes
  • Turner's syndrome, centromere & cosmid probe
  • Whole arm translocation, centromere probes
  • Pericentric chromosome inversion
  • Duchenne muscular dystrophy control, FISH
  • A type of family tree with the parents occupying the centre space surrounded by their progeny with each of the figures appearing to be suffering from some kind of deformity. Engraving.
  • Prader Willi & Angelman's syndromes - probes
  • Interphase cells showing pentameric X
  • XYY syndrome karyotype 47,XYY
  • Aniridia + translocation, FISH & cosmid prob
  • Translocation shown up by cosmid probes
  • People should be open and candid with their doctors about hereditary illnesses, so that the German state can act to eliminate them. Colour lithograph, 1933/1945.
  • Unbalanced translocation 46,XY,t(13;14)
  • Foetal cells in amniotic fluid, + colchicine
  • Leukamia karyotype t(8;14)
  • Balanced translocation 46,XY,t(4;10)
  • Fragile X metaphase spread + nucleus
  • Chorionic villi explants in culture flask
  • XYY syndrome karyotype 46,XYY
  • Fragile X diagnostic test - female carrier
  • Chronic myeloid leukaemia karyotype 9;22
  • Healthy parents with healthy children, representing benefits of the National Socialist policy on the struggle against inherited diseases. Colour lithograph after F.Th. Würbel, 1936.
  • Kayrnes- Sayre Syndrome, glucagon production in pancreas
  • Aniridia + deletion, FISH probes
  • Fragile X pedigree + rflp autoradiograph