39 results filtered with: Genetic disease
- Digital Images
- Online
Inversion in X chromosome
Wessex Reg. Genetics Centre- Digital Images
- Online
Acute myelomonocytic leukaemia +eosinophilia
Wessex Reg. Genetics Centre- Digital Images
- Online
Paracentric chromosome inversion
Wessex Reg. Genetics Centre- Digital Images
- Online
Foetal cells in amniotic fluid, low power LM
Wessex Reg. Genetics Centre- Digital Images
- Online
Foetal cells from amniotic fluid in culture
Wessex Reg. Genetics Centre- Digital Images
- Online
Edward's syndrome karyotype, 47,XY,+18
Wessex Reg. Genetics Centre- Digital Images
- Online
Interphase cells showing pentameric X
Wessex Reg. Genetics Centre- Digital Images
- Online
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
Wessex Reg. Genetics Centre- Digital Images
- Online
Balanced translocation 45,XY,t(21;21)
Wessex Reg. Genetics Centre- Digital Images
- Online
Foetal cells from amniotic fluid, colchicine
Wessex Reg. Genetics Centre- Digital Images
- Online
Down's syndrome karyotype 47,XX,+21
Wessex Reg. Genetics Centre- Digital Images
- Online
Leukaemia karyotype t(4;11) etc
Wessex Reg. Genetics Centre- Digital Images
- Online
Metaphase, deletion on chromosome 15
Wessex Reg. Genetics Centre- Digital Images
- Online
Fragile X chromosome, atomic force microscope
Dr Ben Oostra- Digital Images
- Online
Balanced translocation 46,XY,t(4;10)
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
- Online
Chorionic villi explants in culture flask
Wessex Reg. Genetics Centre- Digital Images
- Online
Abnormal foetal cells in amniotic fluid
Wessex Reg. Genetics Centre- Digital Images
- Online
Pericentric chromosome inversion
Wessex Reg. Genetics Centre- Digital Images
- Online
Acute promyelocytic leukaemia karyotype
Wessex Reg. Genetics Centre- Digital Images
- Online
Duchenne muscular dystrophy carrier female
Wessex Reg. Genetics Centre- Digital Images
- Online
Turner's syndrome karyotype 45,XO. This female lacks the second X chromosome present in the normal karyotype. Symptoms include short stature, neck wbbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The ovaries are reduced to fibrous streaks. Also known as XO syndrome or ovarian short-stature syndrome.
Wessex Reg. Genetics Centre- Digital Images
- Online
Foetal cells in amniotic fluid, + colchicine
Wessex Reg. Genetics Centre- Digital Images
- Online
Chorionic villi samples in petri dish
Wessex Reg. Genetics Centre- Digital Images
- Online
Balanced translocation 45,XY,t(14;21)
Wessex Reg. Genetics Centre