Review log

This is a log of which versions of content pages are checked.

• 17:29, 29 December 2024 Jennelleh talk contribs reviewed a version of GTS5:Turner syndrome ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:12, 11 December 2024)
• 17:28, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Klinefelter syndrome ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:28, 29 December 2024)
• 17:28, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Mosaic variegated aneuploidy (BUB1B, CEP57, TRIP13, BUB1, BUB3) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:28, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Mosaic variegated aneuploidy (BUB1B, CEP57, TRIP13, BUB1, BUB3) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:DDX41-related haematologic tumour predisposition syndrome (DDX41) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:DDX41-related haematologic tumour predisposition syndrome (DDX41) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Rothmund-Thomson syndrome (ANAPC1, RECQL4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Rothmund-Thomson syndrome (ANAPC1, RECQL4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Werner syndrome (WRN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Werner syndrome (WRN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:27, 29 December 2024)
• 17:27, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Bloom syndrome (BLM) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:27, 29 December 2024)
• 17:26, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Polymerase proofreading-associated polyposis (POLD1, POLE) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:26, 29 December 2024)
• 17:26, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Polymerase proofreading-associated polyposis (POLD1, POLE) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:26, 29 December 2024)
• 17:26, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Nijmegen breakage syndrome (NBN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:26, 29 December 2024)
• 17:26, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Nijmegen breakage syndrome (NBN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:26, 29 December 2024)
• 17:26, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:26, 29 December 2024)
• 17:25, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Ataxia-telangiectasia syndrome (ATM) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:25, 29 December 2024)
• 17:25, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Xeroderma Pigmentosum ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:25, 29 December 2024)
• 17:25, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Xeroderma Pigmentosum ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:25, 29 December 2024)
• 17:25, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:MBD4-associated neoplasia syndrome (MBD4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:25, 29 December 2024)
• 17:25, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:MBD4-associated neoplasia syndrome (MBD4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:25, 29 December 2024)
• 17:25, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:NTHL1-related tumour syndrome (NTHL1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:25, 29 December 2024)
• 17:24, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:NTHL1-related tumour syndrome (NTHL1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:24, 29 December 2024)
• 17:24, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:MUTYH-associated polyposis (MUTYH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:24, 29 December 2024)
• 17:24, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:MUTYH-associated polyposis (MUTYH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:24, 29 December 2024)
• 17:23, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Fanconi anaemia (FANC genes) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:23, 29 December 2024)
• 17:23, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:RAD51-related cancer predisposition syndrome (RAD51C, RAD51D) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:23, 29 December 2024)
• 17:22, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:RAD51-related cancer predisposition syndrome (RAD51C, RAD51D) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:22, 29 December 2024)
• 17:19, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:PALB2-related cancer predisposition syndrome (PALB2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:19, 29 December 2024)
• 17:18, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:BRCA-related cancer predisposition syndrome (BRCA1, BRCA2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:18, 29 December 2024)
• 17:17, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:17, 29 December 2024)
• 17:16, 29 December 2024 Jennelleh talk contribs reviewed a version of GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:16, 29 December 2024)
• 17:13, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:13, 29 December 2024)
• 17:13, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:13, 29 December 2024)
• 17:13, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Lynch Syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:13, 29 December 2024)
• 17:12, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Autoimmune lymphoproliferative syndrome (FAS) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:12, 29 December 2024)
• 17:12, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Autoimmune lymphoproliferative syndrome (FAS) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:12, 29 December 2024)
• 17:12, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:CDK4-related melanoma predisposition syndrome (CDK4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:12, 29 December 2024)
• 17:12, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:CDK4-related melanoma predisposition syndrome (CDK4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:12, 29 December 2024)
• 17:11, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:CDKN2A-related tumour predisposition syndrome (CDKN2A) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:11, 29 December 2024)
• 17:11, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:CDKN2A-related tumour predisposition syndrome (CDKN2A) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:11, 29 December 2024)
• 17:11, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Multiple endocrine neoplasia type 4 (CDKN1B) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:11, 29 December 2024)
• 17:11, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Multiple endocrine neoplasia type 4 (CDKN1B) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:11, 29 December 2024)
• 17:11, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Retinoblastoma syndrome (RB1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:11, 29 December 2024)
• 17:11, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Retinoblastoma syndrome (RB1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:11, 29 December 2024)
• 17:10, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Li-Fraumeni syndrome (TP53) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:10, 29 December 2024)
• 17:09, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Hereditary tyrosinaemia type 1 (FAH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:09, 29 December 2024)
• 17:09, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Hereditary tyrosinaemia type 1 (FAH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:09, 29 December 2024)
• 17:09, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (changes reviewed) (revision: 17:09, 29 December 2024)
• 17:09, 29 December 2024 Jennelleh talk contribs automatically reviewed a version of GTS5:Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable]) (revision: 17:09, 29 December 2024)