39 results filtered with: Genetic disease
- Digital Images
- Online
XYY syndrome karyotype 46,XYY
Wessex Reg. Genetics Centre- Digital Images
- Online
Foetal cells from amniotic fluid in culture
Wessex Reg. Genetics Centre- Digital Images
- Online
Klinefelter's syndrome karyotype 47,XXY
Wessex Reg. Genetics Centre- Digital Images
- Online
Diagnostic test for Fragile X, using presence (normal) or absence (Fragile X syndrome) of FMR-1 protein. FMR-1 protein expression in blood cells has been made visible with antibodies against the FMR-1 protein. The presence of FMR-1 protein is made visible as red staining. a: red staining in cells of normal individual. b/c: absence of staining in male patient. d: female patient; one cell is showing staining and in the other cell there is an absence of staining - this individual is a carrier.
Dr Ben Oostra- Digital Images
- Online
Fragile X chromosome, various stains
Dr Ben Oostra- Digital Images
- Online
Triple-X chromosome aberration karyotype
Wessex Reg. Genetics Centre- Digital Images
- Online
Kayrnes- Sayre Syndrome, glucagon production in pancreas
Anne Clark, University of Oxford- Digital Images
- Online
Unbalanced translocation 46,XY,t(21;21)
Wessex Reg. Genetics Centre- Digital Images
- Online
Unbalanced translocation 46,XY,t(13;14)
Wessex Reg. Genetics Centre- Digital Images
- Online
Patau's syndrome karyotype 47,XY,+13
Wessex Reg. Genetics Centre- Digital Images
- Online
Down syndrome human karyotype 47,XY,+21
Wessex Reg. Genetics Centre- Digital Images
- Online
Fragile X metaphase spread
Wessex Reg. Genetics Centre- Digital Images
- Online
Unbalanced translocation 46,XY,t(14;21)
Wessex Reg. Genetics Centre- Digital Images
- Online
Follicular non-Hodgkinson's lymphoma
Wessex Reg. Genetics Centre