88 results filtered with: Wessex Reg. Genetics Centre
- Digital Images
- Online
Turner's stndrome, centromere & cosmid probe
Wessex Reg. Genetics Centre
- Digital Images
- Online
XYY syndrome karyotype 47,XYY
Wessex Reg. Genetics Centre
- 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
Duchenne muscular dystrophy pedigree chart
Wessex Reg. Genetics Centre
- Digital Images
- Online
Acute myelomonocytic leukaemia +eosinophilia
Wessex Reg. Genetics Centre
- Digital Images
- Online
Fragile X pedigree + rflp autoradiograph
Wessex Reg. Genetics Centre
- Digital Images
- Online
Pressure palsy, deletion c'some 17, cosmid
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
Translocation shown using centromere probes
Wessex Reg. Genetics Centre
- Digital Images
- Online
Fragile X pedigree + rflp autoradiograph
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
Prader Willi & Angelman's syndromes - probes
Wessex Reg. Genetics Centre
- Digital Images
- Online
Duchenne muscular dystrophy deletion, FISH
Wessex Reg. Genetics Centre
- Digital Images
- Online
Translocation - use of cosmid probe
Wessex Reg. Genetics Centre
- Digital Images
- Online
Edward's syndrome karyotype, 47,XY,+18
Wessex Reg. Genetics Centre
- Digital Images
- Online
Klinefelter's syndrome karyotype 47,XXY
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