88 results
- Digital Images
- Online
Fragile X metaphase spread + nucleus
Wessex Reg. Genetics Centre- Digital Images
- Online
Fragile X metaphase spread + nucleus
Wessex Reg. Genetics Centre- Digital Images
- Online
Fragile X metaphase spread
Wessex Reg. Genetics Centre- Digital Images
- Online
XYY syndrome karyotype 47,XYY
Wessex Reg. Genetics Centre- Digital Images
- Online
Interphase cells showing pentameric X
Wessex Reg. Genetics Centre- Digital Images
- Online
DiGeorge syndrome - deleted/nondeleted FISH
Wessex Reg. Genetics Centre- Digital Images
- Online
Translocation shown up by cosmid probes
Wessex Reg. Genetics Centre- Digital Images
- Online
Translocation, shown by cosmid probes
Wessex Reg. Genetics Centre- Digital Images
- Online
Duchenne muscular dystrophy pedigree chart
Wessex Reg. Genetics Centre- Digital Images
- Online
Down syndrome human karyotype 47,XY,+21
Wessex Reg. Genetics Centre- Digital Images
- Online
Familial aniridia deletion shown by cosmid
Wessex Reg. Genetics Centre- Digital Images
- Online
Metaphase, deletion on chromosome 15
Wessex Reg. Genetics Centre- Digital Images
- Online
Aniridia + translocation, FISH & cosmid prob
Wessex Reg. Genetics Centre- Digital Images
- Online
Triple-X chromosome aberration karyotype
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
XYY syndrome karyotype 46,XYY
Wessex Reg. Genetics Centre- Digital Images
- Online
Leukamia karyotype t(8;14)
Wessex Reg. Genetics Centre- Digital Images
- Online
Human metaphase, translocation, cosmid probe
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
Inversion in X chromosome
Wessex Reg. Genetics Centre- Digital Images
- Online
Fragile X pedigree + rflp autoradiograph
Wessex Reg. Genetics Centre- Digital Images
- Online
Translocation shown using centromere probes
Wessex Reg. Genetics Centre- Digital Images
- Online
Klinefelter's syndrome karyotype 47,XXY
Wessex Reg. Genetics Centre- Digital Images
- Online
Aniridia + deletion, FISH probes
Wessex Reg. Genetics Centre- Digital Images
- Online
Aniridia, Wilm's tumour, deletion - FISH
Wessex Reg. Genetics Centre