35 results filtered with: Karyotype
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Inversion in X chromosome
Wessex Reg. Genetics Centre
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Acute myelomonocytic leukaemia +eosinophilia
Wessex Reg. Genetics Centre
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Paracentric chromosome inversion
Wessex Reg. Genetics Centre
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Edward's syndrome karyotype, 47,XY,+18
Wessex Reg. Genetics Centre
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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
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Balanced translocation 45,XY,t(21;21)
Wessex Reg. Genetics Centre
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Down's syndrome karyotype 47,XX,+21
Wessex Reg. Genetics Centre
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Leukaemia karyotype t(4;11) etc
Wessex Reg. Genetics Centre
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Chromosome condensation prophase to metaphas
Wessex Reg. Genetics Centre
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Balanced translocation 46,XY,t(4;10)
Wessex Reg. Genetics Centre
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Acute myeloblastic leukaemia karyotype
Wessex Reg. Genetics Centre
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Pericentric chromosome inversion
Wessex Reg. Genetics Centre
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Acute promyelocytic leukaemia karyotype
Wessex Reg. Genetics Centre
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Leukaemia karyotype, acute myelodysplasia
Wessex Reg. Genetics Centre
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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
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Balanced translocation 45,XY,t(14;21)
Wessex Reg. Genetics Centre
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XYY syndrome karyotype 46,XYY
Wessex Reg. Genetics Centre
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Myelodysplasia (leukaemia) karyotype
Wessex Reg. Genetics Centre
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Klinefelter's syndrome karyotype 47,XXY
Wessex Reg. Genetics Centre
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Inheritance of translocations
Wessex Reg. Genetics Centre
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Chronic myeloid leukaemia karyotype 9;22
Wessex Reg. Genetics Centre
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Triple-X chromosome aberration karyotype
Wessex Reg. Genetics Centre
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Balanced translocation 45,XY,t(13;14)
Wessex Reg. Genetics Centre
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Unbalanced translocation 46,XY,t(21;21)
Wessex Reg. Genetics Centre
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Unbalanced translocation 46,XY,t(13;14)
Wessex Reg. Genetics Centre