147 results
- Digital Images
- Online
Patau's syndrome karyotype 47,XY,+13
Wessex Reg. Genetics Centre- Digital Images
- Online
Human karyotype showing translocation between chromosomes 14 and 21, t(14;21). This is a balanced translocation - the cell retains a normal complement of genetic information.
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- Archives and manuscripts
- Online
Typescript draft of 'Comparative chromosome map between the Japanese raccoon dog, Arctic fox, red fox and domestic dog and its implications for the ancestral canid karyotype'
Date: Mar 2000Reference: UGC 188/4/1/31/2Part of: Papers of Malcolm Andrew Ferguson-Smith, geneticist, Professor of Medical Genetics, University of Glasgow, Scotland- Archives and manuscripts
- Online
Typescript draft of 'Comparative chromosome map between the Japanese raccoon dog, Arctic fox, red fox and domestic dog and its implications for the ancestral canid karyotype'
Date: 2000Reference: UGC 188/4/1/31/1Part of: Papers of Malcolm Andrew Ferguson-Smith, geneticist, Professor of Medical Genetics, University of Glasgow, Scotland- Archives and manuscripts
- Online
'Generation of a multicolor karyotype of the human chromosome complement using fluorescence in situ hydridization and spectral imaging,' with E Schrock et al.
Date: 1996Reference: UGC 188/4/1/12Part of: Papers of Malcolm Andrew Ferguson-Smith, geneticist, Professor of Medical Genetics, University of Glasgow, Scotland- Archives and manuscripts
- Online
'Cross species colour segmenting: a novel tool in human karyotype analysis,' with S Müller et al. in Cytometry 33, (1998), pp. 445-452
Date: 1998Reference: UGC 188/4/1/19Part of: Papers of Malcolm Andrew Ferguson-Smith, geneticist, Professor of Medical Genetics, University of Glasgow, Scotland- Archives and manuscripts
'Comparative chromosome map between the Japanese raccoon dog, Arctic fox, red fox and domestic dog and its implications for the ancestral canid karyotype,' with Alexander S Graphodatsky et al.
Date: 2000Reference: UGC 188/4/1/31Part of: Papers of Malcolm Andrew Ferguson-Smith, geneticist, Professor of Medical Genetics, University of Glasgow, Scotland- Archives and manuscripts
Photographs of Familial Prints and Karyotypes for J H Edwards
Date: c.1962Reference: PENROSE/2/42/8/3/2Part of: L. S. Penrose Papers- Archives and manuscripts
Dermatoglyphic Reports, Chromosome Reports, Dermatoglyphs and Karyotypes for J Luder
Date: 1962Reference: PENROSE/2/42/8/3/19Part of: L. S. Penrose Papers- Archives and manuscripts
Registry of Abnormal Karyotypes in Cases up to 1 September 1964
Date: Sep 1964Reference: PENROSE/2/41/13/1/21Part of: L. S. Penrose Papers- Books
Chromosome identification : technique and applications in biology and medicine proceedings of the twenty-third Nobel Symposium held September 25-27, 1972 at the Royal Swedish Academy of Sciences, Stockholm / editors, Torbjörn Caspersson and Lore Zech.
Nobel Symposium 1972 : Stockholm, Sweden)Date: [1973]- Digital Images
- Online
Follicular non-Hodgkinson's lymphoma
Wessex Reg. Genetics Centre- Books
- Online
Sravnitelʹnai︠a︡︠ t︡sitogenetika i kariosistematika mlekopitai︠u︡shchikh / V.N. Orlov, N. Sh. Bulatova.
Orlov, V. N. (Viktor Nikolaevich)Date: 1983- Digital Images
- Online
Hyperdiploid acute lymphoblastic leukaemia
Wessex Reg. Genetics Centre- Digital Images
- Online
Chromosome condensation prophase to metaphas
Wessex Reg. Genetics Centre- Digital Images
- Online
Acute myelomonocytic leukaemia +eosinophilia
Wessex Reg. Genetics Centre- Digital Images
- Online
Inheritance of translocations
Wessex Reg. Genetics Centre- Digital Images
- Online
Inversion in X chromosome
Wessex Reg. Genetics Centre- Digital Images
- Online
Balanced translocation 45,XY,t(13;14)
Wessex Reg. Genetics Centre- Digital Images
- Online
Paracentric chromosome inversion
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
Balanced translocation 46,XY,t(4;10)
Wessex Reg. Genetics Centre- Digital Images
- Online
Pericentric chromosome inversion
Wessex Reg. Genetics Centre