|
XB--482020
Papers associated with runx2 (and Disease Ontology)
Results 1 - 2 of 2 results
Page(s): 1
Sort Newest To Oldest | Sort Oldest To Newest |
ROMK expression remains unaltered in a mouse model of familial hyperkalemic hypertension caused by the CUL3Δ403-459 mutation., Murthy M, Kurz T, O'Shaughnessy KM., Physiol Rep. July 1, 2016; 4 (13): ![]() |
|
Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning., Fakhro KA, Choi M, Ware SM, Belmont JW, Towbin JA, Lifton RP, Khokha MK, Brueckner M., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20. ![]() |
Page(s): 1