File:Inheritance pattern in Huntington's Disease.jpeg: Revision history

From Embryology

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

28 October 2011

13 October 2011

6 October 2011

2 October 2011

22 September 2011

  • curprev 12:2412:24, 22 September 2011Z3290270 talk contribs 271 bytes +271 Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome. Illustration by: z3290270 Inspiration: Yale Madical group - Yale Sc