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(==Trisomy X== Trisomy X, 3 copies of the X chromosome identified in a single cell nucleus by fluorescent in situ hybridisation (FISH) analysis. ===Reference=== <pubmed>23162306</pubmed>| [http://www.ijhg.com/article.asp?issn=0971-6866;year=2012;vol...)
 
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Trisomy X, 3 copies of the X chromosome identified in a single cell nucleus by fluorescent in situ hybridisation (FISH) analysis.
Trisomy X, 3 copies of the X chromosome identified in a single cell nucleus by fluorescent in situ hybridisation (FISH) analysis.


:'''Links:''' [[Trisomy X]] | [[Abnormal_Development_-_Genetic|Abnormal Development - Genetic]] |


===Reference===
===Reference===

Revision as of 20:36, 24 December 2013

Trisomy X

Trisomy X, 3 copies of the X chromosome identified in a single cell nucleus by fluorescent in situ hybridisation (FISH) analysis.


Links: Trisomy X | Abnormal Development - Genetic |

Reference

<pubmed>23162306</pubmed>| Indian J Hum Genet.


Copyright

CC BY-NC-SA 3.0


Original Figure 2 cropped, resized and labelled. IndianJHumGenet_2012_18_2_246_100790_u2.jpg

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current20:34, 24 December 2013Thumbnail for version as of 20:34, 24 December 2013400 × 352 (15 KB)Z8600021 (talk | contribs)==Trisomy X== Trisomy X, 3 copies of the X chromosome identified in a single cell nucleus by fluorescent in situ hybridisation (FISH) analysis. ===Reference=== <pubmed>23162306</pubmed>| [http://www.ijhg.com/article.asp?issn=0971-6866;year=2012;vol...

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