88 results
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Prader Willi & Angelman syndromes - FISH
Wessex Reg. Genetics Centre- Digital Images
- Online
Huntington's chorea pedigree, constructed from
Wessex Reg. Genetics Centre- Digital Images
- Online
Patau's syndrome karyotype 47,XY,+13
Wessex Reg. Genetics Centre- Digital Images
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Foetal cells from amniotic fluid in culture
Wessex Reg. Genetics Centre- Digital Images
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Duchenne muscular dystrophy deletion, FISH
Wessex Reg. Genetics Centre- Digital Images
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Edward's syndrome karyotype, 47,XY,+18
Wessex Reg. Genetics Centre- Digital Images
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Foetal cells from amniotic fluid, colchicine
Wessex Reg. Genetics Centre- Digital Images
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Down's syndrome karyotype 47,XX,+21
Wessex Reg. Genetics Centre- Digital Images
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Duchenne muscular dystrophy control, FISH
Wessex Reg. Genetics Centre- Digital Images
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Down syndrome human karyotype 47,XY,+21
Wessex Reg. Genetics Centre- Digital Images
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Fragile X metaphase spread
Wessex Reg. Genetics Centre- Digital Images
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Prader Willi & Angelman's syndromes - probes
Wessex Reg. Genetics Centre- Digital Images
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Foetal cells from amniotic fluid in culture
Wessex Reg. Genetics Centre- Digital Images
- Online
Prader Willi & Angelman's syndromes - probes
Wessex Reg. Genetics Centre- Digital Images
- Online
Abnormal foetal cells in amniotic fluid
Wessex Reg. Genetics Centre- Digital Images
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Acute promyelocytic leukaemia karyotype
Wessex Reg. Genetics Centre- Digital Images
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Acute myelomonocytic leukaemia +eosinophilia
Wessex Reg. Genetics Centre- Digital Images
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Foetal cells in amniotic fluid, low power LM
Wessex Reg. Genetics Centre- Digital Images
- Online
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- Digital Images
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Chorionic villi explants in culture flask
Wessex Reg. Genetics Centre- Digital Images
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Duchenne muscular dystrophy carrier female
Wessex Reg. Genetics Centre- Digital Images
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Foetal cells in amniotic fluid, + colchicine
Wessex Reg. Genetics Centre- Digital Images
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Chorionic villi samples in petri dish
Wessex Reg. Genetics Centre- Digital Images
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Genetics frame of reference - the size of various genetic components, including DNA, a base pair, various sizes of deletions, chromosomes and genes are listed and compared with more familiar objects such as the Solar System, planets, cities, hospitals, wards, and so on.
Wessex Reg. Genetics Centre- Digital Images
- Online
Human karyotype showing translocation between chromosomes 14 and 21, t(14;21). This is a balanced translocation - the cell retains a normal complement of genetic information.
Wessex Reg. Genetics Centre