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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.

Links: Trisomy X | Abnormal Development - Genetic |

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

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

Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan

	Gwalagizhi	Nyangagi	Dimensions	User	Comment
current	21:34, 24 December 2013		400 × 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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