Pages that link to "Q67436928"

The following pages link to Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BudR treatment (Q67436928):

Displaying 7 items.

• Inactivation centers in the human X chromosome. (Q35202116) (← links)
• Duplication of the short arm of the X chromosome in mother and daughter (Q36783772) (← links)
• Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features (Q40550174) (← links)
• The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis (Q41234841) (← links)
• Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion (Q52075472) (← links)
• A note on the Xp- (Q66942386) (← links)
• Partial short arm deletion of the X chromosome 46,X,del(X)(qter = to p21:) (Q71142655) (← links)