File:TurnerSyndromeXChromosomeFormations.jpg: Difference between revisions
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==Turner Syndrome - X Chromosome Variations== | ==Turner Syndrome - X Chromosome Variations== | ||
Figure shows Turner syndrome variations of the second X chromosome. | |||
A. Completely absent (45,X) | |||
B. Partially absent | |||
C. Forms an isochromosome (isoXq), possessing a long arm duplication (q) and being devoid of a short arm (p) | |||
D. In a ring formation (rX) | |||
E. Is devoid of the homeobox gene, SHOX (short stature homeobox), the deletion being prior to the junction between Xp22.2 and Xp22.3 | |||
Revision as of 20:47, 19 September 2011
Turner Syndrome - X Chromosome Variations
Figure shows Turner syndrome variations of the second X chromosome.
A. Completely absent (45,X) B. Partially absent C. Forms an isochromosome (isoXq), possessing a long arm duplication (q) and being devoid of a short arm (p) D. In a ring formation (rX) E. Is devoid of the homeobox gene, SHOX (short stature homeobox), the deletion being prior to the junction between Xp22.2 and Xp22.3
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