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

OriginalsprogEngelsk
Publikationsdato2009
StatusUdgivet - 2009
BegivenhedEuropean Human Genetics Conference, Vienna 2009. - Vienna, Østrig
Varighed: 29 nov. 2010 → …

Konference

KonferenceEuropean Human Genetics Conference, Vienna 2009.
Land/OmrådeØstrig
ByVienna
Periode29/11/2010 → …

Citationsformater