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The following pages link to Template:Ombox:

Displaying 50 items.

• GTS5:Schimmelpenning-Feuerstein-Mims (HRAS, KRAS) (transclusion) (← links)
• GTS5:Carney complex (PRKAR1A, PDE8B, PDE11A) (transclusion) (← links)
• GTS5:PROS syndrome (PIK3CA) (transclusion) (← links)
• GTS5:Gastric Adenocarcinoma and Proximal Polyposis of Stomach - GAPPS (APC promoter) (transclusion) (← links)
• GTS5:AXIN2-associated polyposis (AXIN2) (transclusion) (← links)
• GTS5:Serrated polyposis (RNF43) (transclusion) (← links)
• GTS5:WT1 related tumour predisposition syndrome (WT1) (transclusion) (← links)
• GTS5:Hereditary mixed polyposis syndrome (GREM1) (transclusion) (← links)
• GTS5:Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161) (transclusion) (← links)
• GTS5:SMO-related Curry-Jones syndrome (SMO) (transclusion) (← links)
• GTS5:ELP1-related medulloblastoma predisposition syndrome(ELP1) (transclusion) (← links)
• GTS5:Osteochondromatosis (EXT1, EXT2) (transclusion) (← links)
• GTS5:Brooke-Spiegler syndrome (CYLD) (transclusion) (← links)
• GTS5:Tuberous sclerosis (TSC1, TSC1) (transclusion) (← links)
• GTS5:Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD) (transclusion) (← links)
• GTS5:Multiple endocrine neoplasia type 5, MAX related tumours (MAX) (transclusion) (← links)
• GTS5:MAFA-related familial insulinomatosis (MAFA) (transclusion) (← links)
• GTS5:Birt-Hogg-Dube syndrome (FLCN) (transclusion) (← links)
• GTS5:Familial chordoma (TBXT) (transclusion) (← links)
• GTS5:Hyperparathyroidism jaw tumour syndrome (CDC73) (transclusion) (← links)
• GTS5:Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH) (transclusion) (← links)
• GTS5:Hereditary tyrosinaemia type 1 (FAH) (transclusion) (← links)
• GTS5:Retinoblastoma syndrome (RB1) (transclusion) (← links)
• GTS5:Multiple endocrine neoplasia type 4 (CDKN1B) (transclusion) (← links)
• GTS5:CDKN2A-related tumour predisposition syndrome (CDKN2A) (transclusion) (← links)
• GTS5:CDK4-related melanoma predisposition syndrome (CDK4) (transclusion) (← links)
• GTS5:Autoimmune lymphoproliferative syndrome (FAS) (transclusion) (← links)
• GTS5:Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6) (transclusion) (← links)
• GTS5:RAD51-related cancer predisposition syndrome (RAD51C, RAD51D) (transclusion) (← links)
• GTS5:MUTYH-associated polyposis (MUTYH) (transclusion) (← links)
• GTS5:NTHL1-related tumour syndrome (NTHL1) (transclusion) (← links)
• GTS5:MBD4-associated neoplasia syndrome (MBD4) (transclusion) (← links)
• GTS5:Xeroderma Pigmentosum (transclusion) (← links)
• GTS5:Nijmegen breakage syndrome (NBN) (transclusion) (← links)
• GTS5:Polymerase proofreading-associated polyposis (POLD1, POLE) (transclusion) (← links)
• GTS5:Werner syndrome (WRN) (transclusion) (← links)
• GTS5:Rothmund-Thomson syndrome (ANAPC1, RECQL4) (transclusion) (← links)
• GTS5:DDX41-related haematologic tumour predisposition syndrome (DDX41) (transclusion) (← links)
• GTS5:Mosaic variegated aneuploidy (BUB1B, CEP57, TRIP13, BUB1, BUB3) (transclusion) (← links)
• GTS5:Dyskeratosis congenita (DKC1, TERT, TERC, TINF2, Other IBMFS genes) (transclusion) (← links)
• GTS5:POT1 and Shelterin-related tumour predisposition syndrome (POT1, ACD, TERF2IP, TERT promoter) (transclusion) (← links)
• GTS5:Beckwith-Wiedemann spectrum (IGF2; CDKN1C) (transclusion) (← links)
• GTS5:Enchondromatosis (IDH1, IDH2) (transclusion) (← links)
• GTS5:Rhabdoid tumour predisposition syndrome (SMARCB1, SMARCA4) (transclusion) (← links)
• GTS5:Schwannomatosis (SMARCB1, LZTR1) (transclusion) (← links)
• GTS5:Clear cell meningioma predisposition syndrome (SMARCE1) (transclusion) (← links)
• GTS5:Weaver syndrome (EZH2) (transclusion) (← links)
• GTS5:MicroRNA processor tumour predisposition syndromes (DROSHA, DGCR8) (transclusion) (← links)
• GTS5:Goldenhar syndrome (MYT1, SF3B2) (transclusion) (← links)
• GTS5:BAP1-related tumour predisposition syndrome (BAP1) (transclusion) (← links)