Terms: = Leukemia AND FANCD2, FANCD, 2177, ENSG00000144554, FLJ23826, FAD, FACD, FA4, FA-D2, FAD2, DKFZp762A223 AND Clinical Outcome
2 results:
1. Whole exome sequencing identifies a novel fancd2 gene splice site mutation associated with disease progression in chronic myeloid leukemia: Implication in targeted therapy of advanced phase CML.
Absar M; Mahmood A; Akhtar T; Basit S; Ramzan K; Jameel A; Afzal S; Ullah A; Qureshi K; Alanazi N; Iqbal Z
Pak J Pharm Sci; 2020 May; 33(3(Special)):1419-1426. PubMed ID: 33361032
[TBL] [Abstract] [Full Text] [Related]
2. Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
Faivre L; Guardiola P; Lewis C; Dokal I; Ebell W; Zatterale A; Altay C; Poole J; Stones D; Kwee ML; van Weel-Sipman M; Havenga C; Morgan N; de Winter J; Digweed M; Savoia A; Pronk J; de Ravel T; Jansen S; Joenje H; Gluckman E; Mathew CG
Blood; 2000 Dec; 96(13):4064-70. PubMed ID: 11110674
[TBL] [Abstract] [Full Text] [Related]
