Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations.

L Hansen, AK Riis, HD Hove, E Lauridsen, Hans Rudolf Lytchoff Eiberg, Sven Kreiborg

Original languageEnglish
Publication date2009
Publication statusPublished - 2009
EventEuropean Human Genetics Conference, Vienna 2009. - Vienna, Austria
Duration: 29 Nov 2010 → …

Conference

ConferenceEuropean Human Genetics Conference, Vienna 2009.
Country/TerritoryAustria
CityVienna
Period29/11/2010 → …

Cite this