File:TurnerSyndromeXChromosomeFormations.jpg: Difference between revisions
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A. Completely absent (45,X) | A. Completely absent (45,X) | ||
B. Partially absent | B. Partially absent | ||
C. Forms an isochromosome (isoXq), possessing a long arm duplication (q) and being devoid of a short arm (p) | 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) | 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 | 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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