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Turner's stndrome, centromere & cosmid probe

XYY syndrome karyotype 47,XYY

Normal human male metaphase, Y banding

Inversion in X chromosome

Duchenne muscular dystrophy pedigree chart

Acute myelomonocytic leukaemia +eosinophilia

Fragile X pedigree + rflp autoradiograph

Pressure palsy, deletion c'some 17, cosmid

Paracentric chromosome inversion

Foetal cells in amniotic fluid, low power LM

Foetal cells from amniotic fluid in culture

Translocation shown using centromere probes

Down syndrome human karyotype 47,XY,+21

Familial aniridia deletion shown by cosmid

Prader Willi & Angelman's syndromes - probes

Duchenne muscular dystrophy deletion, FISH

Translocation - use of cosmid probe

Edward's syndrome karyotype, 47,XY,+18

Klinefelter's syndrome karyotype 47,XXY

Interphase cells showing pentameric X

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(21;21)

Foetal cells from amniotic fluid, colchicine

Down's syndrome karyotype 47,XX,+21

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Turner's stndrome, centromere & cosmid probe

XYY syndrome karyotype 47,XYY

Normal human male metaphase, Y banding

Inversion in X chromosome

Duchenne muscular dystrophy pedigree chart

Acute myelomonocytic leukaemia +eosinophilia

Fragile X pedigree + rflp autoradiograph

Pressure palsy, deletion c'some 17, cosmid

Paracentric chromosome inversion

Foetal cells in amniotic fluid, low power LM

Foetal cells from amniotic fluid in culture

Translocation shown using centromere probes

Fragile X pedigree + rflp autoradiograph

Down syndrome human karyotype 47,XY,+21

Familial aniridia deletion shown by cosmid

Prader Willi & Angelman's syndromes - probes

Duchenne muscular dystrophy deletion, FISH

Translocation - use of cosmid probe

Edward's syndrome karyotype, 47,XY,+18

Klinefelter's syndrome karyotype 47,XXY

Interphase cells showing pentameric X

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(21;21)

Foetal cells from amniotic fluid, colchicine

Down's syndrome karyotype 47,XX,+21