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

Research output: Contribution to conferenceConference abstract for conferenceResearch

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.
CountryAustria
CityVienna
Period29/11/2010 → …

ID: 21573494