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 conference › Conference abstract for conference › Research
Original language | English |
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Publication date | 2009 |
Publication status | Published - 2009 |
Event | European Human Genetics Conference, Vienna 2009. - Vienna, Austria Duration: 29 Nov 2010 → … |
Conference
Conference | European Human Genetics Conference, Vienna 2009. |
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Country | Austria |
City | Vienna |
Period | 29/11/2010 → … |
ID: 21573494