Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M A, Rooimans"'
Autor:
M A, Hermsen, Y, Xie, M A, Rooimans, G A, Meijer, J P, Baak, J T, Plukker, F, Arwert, H, Joenje
Publikováno v:
Familial cancer. 1(1)
Fanconi anemia (FA) is an autosomal recessive syndrome with a marked predisposition to malignancies, in particular acute myeloid leukemia and squamous cell carcinoma of the oral cavity. We examined oral squamous cell carcinoma tissue from two FA pati
Autor:
J R, Lo Ten Foe, M L, Kwee, M A, Rooimans, A B, Oostra, A J, Veerman, M, van Weel, R M, Pauli, N T, Shahidi, I, Dokal, I, Roberts, C, Altay, E, Gluckman, R A, Gibson, C G, Mathew, F, Arwert, H, Joenje
Publikováno v:
European journal of human genetics : EJHG. 5(3)
Approximately 25% of patients with Fanconi anemia (FA) have evidence of spontaneously occurring mosaicism as manifest by the presence of two subpopulations of lymphocytes, one of which is hypersensitive to cross-linking agents (e.g. mitomycin C) whil
Publikováno v:
Human mutation. 7(3)
Autor:
H, Joenje, J R, Lo ten Foe, A B, Oostra, C G, van Berkel, M A, Rooimans, T, Schroeder-Kurth, R D, Wegner, J J, Gille, M, Buchwald, F, Arwert
Publikováno v:
Blood. 86(6)
Fanconi anemia (FA) is an autosomal recessive disease with diverse clinical symptoms, life-threatening progressive panmyelopathy, and cellular hypersensitivity to cross-linking agents. Currently, 4 genetic subtypes or complementation groups (FA-A thr