neoplasm
• the average maximal diameter of macroadenomas was larger than in double heterozygous controls
|
• at 120 days of age, exhibited a 2-fold increase in the multiplicity of macroadenomas along the entire GI tract compared to double heterozygous mutant controls, however no difference in the mean or maximal lifespan compared to controls
|
• mutants always developed tumors in the large intestine, a site that is inconsistently affected in double heterozygous controls
|
digestive/alimentary system
• mutants always developed tumors in the large intestine, a site that is inconsistently affected in double heterozygous controls
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
Rothmund-Thomson syndrome | DOID:2732 |
OMIM:268400 |
J:97101 |