File:Turner Syndrome X Chromosome Variations.jpg: Difference between revisions
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Revision as of 10:53, 17 May 2016
Turner Syndrome - X Chromosome Variations
Figure shows Turner syndrome variations of the second X chromosome.
- Completely absent (45,X)
- Partially absent
- Forms an isochromosome (isoXq), possessing a long arm duplication (q) and being devoid of a short arm (p)
- In a ring formation (rX)
- 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>
Assessment
+ Image is relevant to the project and fulfils the student drawn image criteria. + Citation and student disclaimer included.
- Note - This image was originally uploaded as part of a student project and may contain inaccuracies in either description or acknowledgements. Students have been advised in writing concerning the reuse of content and may accidentally have misunderstood the original terms of use. If image reuse on this non-commercial educational site infringes your existing copyright, please contact the site editor for immediate removal.
Cite this page: Hill, M.A. (2024, May 7) Embryology Turner Syndrome X Chromosome Variations.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Turner_Syndrome_X_Chromosome_Variations.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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current | 16:24, 20 September 2011 | 977 × 1,434 (130 KB) | Z3217345 (talk | contribs) | ==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 |
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