Revision history of "Achondroplasia"

From bonepath

Jump to: navigation, search
(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)

Diff selection: mark the radio boxes of the versions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with current version, (last) = difference with preceding version, M = minor edit.

  • (cur) (last) 20:19, 18 September 2011 Cmvs (Talk | contribs) (3,864 bytes) (New page: Achondroplasia is a congenital condition resulting in dwarfism. The abnormality has been traced to a mutation of the FGFR3 gene on chromosome 4 (Shiang et al. 2004). As the condition follo...)
(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)
Personal tools