Standard
Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations. / Hansen, L; Riis, AK; Hove, HD; Lauridsen, E; Eiberg, Hans Rudolf Lytchoff; Kreiborg, Sven.
2009. Abstract from European Human Genetics Conference, Vienna 2009., Vienna, Austria.
Research output: Contribution to conference › Conference abstract for conference › Research
Harvard
Hansen, L, Riis, AK, Hove, HD, Lauridsen, E, Eiberg, HRL & Kreiborg, S 2009, 'Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations.', European Human Genetics Conference, Vienna 2009., Vienna, Austria, 29/11/2010.
APA
Hansen, L., Riis, AK., Hove, HD., Lauridsen, E., Eiberg, H. R. L., & Kreiborg, S. (2009). Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations.. Abstract from European Human Genetics Conference, Vienna 2009., Vienna, Austria.
Vancouver
Hansen L, Riis AK, Hove HD, Lauridsen E, Eiberg HRL, Kreiborg S. Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations.. 2009. Abstract from European Human Genetics Conference, Vienna 2009., Vienna, Austria.
Author
Hansen, L ; Riis, AK ; Hove, HD ; Lauridsen, E ; Eiberg, Hans Rudolf Lytchoff ; Kreiborg, Sven. / Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations. Abstract from European Human Genetics Conference, Vienna 2009., Vienna, Austria.
Bibtex
@conference{febd4500b08511df825b000ea68e967b,
title = "Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations.",
author = "L Hansen and AK Riis and HD Hove and E Lauridsen and Eiberg, {Hans Rudolf Lytchoff} and Sven Kreiborg",
year = "2009",
language = "English",
note = "null ; Conference date: 29-11-2010",
}
RIS
TY - ABST
T1 - Analysis of RUNX2 in a Danish cohort of cleidocranial dysplasia patients revealed two large chromosomal deletions and 14 pathogenic point mutations.
AU - Hansen, L
AU - Riis, AK
AU - Hove, HD
AU - Lauridsen, E
AU - Eiberg, Hans Rudolf Lytchoff
AU - Kreiborg, Sven
PY - 2009
Y1 - 2009
M3 - Conference abstract for conference
Y2 - 29 November 2010
ER -
