88 results filtered with: Wessex Reg. Genetics Centre
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Leukaemia karyotype t(4;11) etc
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Chromosome condensation prophase to metaphas
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Metaphase, deletion on chromosome 15
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Aniridia + deletion, FISH probes
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Translocation shown up by cosmid probe
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Balanced translocation 46,XY,t(4;10)
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Duchenne muscular dystrophy control, FISH
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Duchenne muscular dystrophy - normal female, chromosomes have been highlighted by a fluorescent probe for exon 45/47 (note the double yellow band). This disorder is caused by a recessive gene on the X chromosome, so is normally shown only by males, who lack a second X chromosome. The condition starts with difficulty in walking and climbing stairs in early childhood, usually resulting in confinement to a wheelchair by the age of 10, with death from respiratory infection or cardiac failure by about the age of 20.
Wessex Reg. Genetics Centre
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Aniridia, Wilm's tumour, deletion - FISH
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Chorionic villi explants in culture flask
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DiGeorge syndrome - 22q11deletion - FISH
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Abnormal foetal cells in amniotic fluid
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Acute myeloblastic leukaemia karyotype
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Pericentric chromosome inversion
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Acute promyelocytic leukaemia karyotype
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Fragile X metaphase spread
Wessex Reg. Genetics Centre
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Duchenne muscular dystrophy carrier female
Wessex Reg. Genetics Centre
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Leukaemia karyotype, acute myelodysplasia
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Prader Willi & Angelman syndromes - FISH
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Unbalanced translocation, cosmid probe
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Normal female 46,XX human karyotype
Wessex Reg. Genetics Centre
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Aniridia + translocation, FISH & cosmid prob
Wessex Reg. Genetics Centre
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Triple-X chromosome aberration karyotype
Wessex Reg. Genetics Centre
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Normal male 46,XY human karyotype
Wessex Reg. Genetics Centre
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Huntington's chorea pedigree, constructed from
Wessex Reg. Genetics Centre