Information for "An incident record of an affected individual together with 1st phenotype involving papillary hypothyroid carcinoma along with heterochronous multiprimary tumor holding germline MUTYH Arg19Gly286Glu mutations"
From EECH Central
Basic information
| Display title | An incident record of an affected individual together with 1st phenotype involving papillary hypothyroid carcinoma along with heterochronous multiprimary tumor holding germline MUTYH Arg19Gly286Glu mutations |
| Default sort key | An incident record of an affected individual together with 1st phenotype involving papillary hypothyroid carcinoma along with heterochronous multiprimary tumor holding germline MUTYH Arg19Gly286Glu mutations |
| Page length (in bytes) | 3,707 |
| Page ID | 1312375 |
| Page content language | English (en) |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 0 |
Page protection
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
Edit history
| Page creator | Waspdoctor2 (Talk | contribs) |
| Date of page creation | 10:35, 28 March 2024 |
| Latest editor | Waspdoctor2 (Talk | contribs) |
| Date of latest edit | 10:35, 28 March 2024 |
| Total number of edits | 1 |
| Total number of distinct authors | 1 |
| Recent number of edits (within past 90 days) | 1 |
| Recent number of distinct authors | 1 |
