Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | |
---|---|---|---|
Heterozygous NOTCH1 deletion associated with variable congenital heart defects Journal:Clinical Genetics | 2021 | ||
Overgrowth with increased proliferation of fibroblast and matrix metalloproteinse activity related to reduced T1MP1: a new syndrome Proceeding/Conference:32nd Annual David W. Smith Workshop | 2011 |