File:TurnerSyndromeXChromosomeFormations.jpg: Difference between revisions

From Embryology
 
(One intermediate revision by the same user not shown)
Line 15: Line 15:
Image drawn by --[[User:Z3217345|z3217345]] 21:38, 19 September 2011 (EST).
Image drawn by --[[User:Z3217345|z3217345]] 21:38, 19 September 2011 (EST).


== References ==
=== References ===


P Saenger, K A Wikland, G S Conway, M Davenport, C H Gravholt, R Hintz, O Hovatta, M Hultcrantz, K Landin-Wilhelmsen, A Lin, B Lippe, A M Pasquino, M B Ranke, R Rosenfeld, M Silberbach, Fifth International Symposium on Turner Syndrome Recommendations for the diagnosis and management of Turner syndrome. J. Clin. Endocrinol. Metab.: 2001, 86(7);3061-9 PMID:11443168
<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>

File history

Click on a date/time to view the file as it appeared at that time.

Date/TimeThumbnailDimensionsUserComment
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==

There are no pages that use this file.

Metadata