| 02/10/08 - 07:06 AM  
 
   
 
|   #5 |
wrote: Gonadal dysgenesis, XY female type, is associated with point mutations or deletions of the SRY gene ,but also in some cases with changes in the X chromosome 46,X,i(Xp) 'i(Xp)' is for isochromasis on short arm of X ,causing Xp duplication Small deletions in the short arm of the Y chromosome can result in 46,XY females does any one have any idea about what is this??!!! and if yes, would you explain please...thanx
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