73 results filtered with: Chromosome
- Digital Images
- Online
Human HeLa cancer cells, mitosis
Paul Andrews/Univ. Dundee- Digital Images
- Online
Normal human male metaphase, Y banding
Wessex Reg. Genetics Centre- 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
Human HeLa cancer cells, prometaphase
Paul Andrews/Univ. Dundee- Digital Images
- Online
Human HeLa cancer cell, tripolar mitosis
Paul Andrews/Univ. Dundee- Digital Images
- Online
Human HeLa cancer cells, cytokinesis
Paul Andrews/Univ. Dundee- Digital Images
- Online
Edward's syndrome karyotype, 47,XY,+18
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
Down's syndrome karyotype 47,XX,+21
Wessex Reg. Genetics Centre- Digital Images
- Online
Human HeLa cancer cell chromosome rosettes
Paul Andrews/Univ. Dundee- Digital Images
- Online
Leukaemia karyotype t(4;11) etc
Wessex Reg. Genetics Centre- Digital Images
- Online
Chromosome condensation prophase to metaphas
Wessex Reg. Genetics Centre- Digital Images
- Online
Xenopus cancer kidney cells, interphase
Paul Andrews/Univ. Dundee- Digital Images
- Online
Metaphase, deletion on chromosome 15
Wessex Reg. Genetics Centre- Digital Images
- Online
Human HeLa cancer cells, stages of mitosis
William J Moore/Univ. Dundee- Digital Images
- Online
Human cancer cell
Elena Knatko/Univ. Dundee- Digital Images
- Online
Fragile X chromosome, atomic force microscope
Dr Ben Oostra- Digital Images
- Online
Human HeLa cancer cell in prometaphase of mitosis
William J Moore/Univ. Dundee- 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
Acute myeloblastic leukaemia karyotype
Wessex Reg. Genetics Centre- Digital Images
- Online
Xenopus cancer kidney cells, anaphase
Paul Andrews/Univ. Dundee