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All of Wellcome Collection, including our library, café and shop, will be closed on Monday 4 November for staff training. We will open again as usual on Tuesday 5 November.

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Turner's stndrome, centromere & cosmid probe

XYY syndrome karyotype 47,XYY

Duchenne muscular dystrophy pedigree chart

Fragile X pedigree + rflp autoradiograph

Pressure palsy, deletion c'some 17, cosmid

Fragile X diagnostic test - normal

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

Klinefelter's syndrome karyotype 47,XXY

Aniridia + deletion, FISH probes

Translocation shown up by cosmid probe

Duchenne muscular dystrophy control, FISH

Aniridia, Wilm's tumour, deletion - FISH

DiGeorge syndrome - 22q11deletion - FISH

Acute myeloblastic leukaemia karyotype

Fragile X metaphase spread

Fragile X diagnostic test - male, no stain

Leukaemia karyotype, acute myelodysplasia

Prader Willi & Angelman syndromes - FISH

Unbalanced translocation, cosmid probe

Aniridia + translocation, FISH & cosmid prob

Triple-X chromosome aberration karyotype

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