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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
Image drawn by --[[User:Z3217345|z3217345]] 21:38, 19 September 2011 (EST).
=== References ===
<pubmed>11443168</pubmed>

Latest revision as of 14:37, 20 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

Image drawn by --z3217345 21:38, 19 September 2011 (EST).

References

<pubmed>11443168</pubmed>

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current20:41, 19 September 2011Thumbnail for version as of 20:41, 19 September 2011718 × 1,436 (107 KB)Z3217345 (talk | contribs)==Turner Syndrome - X Chromosome Variations==

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