• Heterogeneous Spectrum Of Mutations In The Fanconi Anaemia Group A Gene 

      Wijker, M; Morgan, NV; Herterich, S; van Berkel, CGM; Tipping, AJ; Gross, HJ; Gille, JJP; Pals, G; Savino, M; Altay, C; Mohan, S; Dokal, I; Cavenagh, J; Marsh, J; Van Weel, M; Ortega, JJ; Schuler, D; Samochatova, E; Karwacki, M; Bekassy, AN; Abecasis, M; Ebell, W; Kwee, ML; de Ravel, T; Gibson, RA; Gluckman, E; Arwert, F; Joenje, H; Savoia, A; Hoehn, H; Pronk, JC; Mathew, CG (Stockton Press, 1999)
      Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chromosomal fragility, bone-marrow failure, congenital abnormalities and cancer. The gene for complementation group A (FAA), ...
    • Results of the Combined Treatment of Pediatric Intraspinal Tumors 

      Dincer, F.; Dincer, C.; Baskaya, MK (Stockton Press, 1992)
      In this article 98 patients with paediatric intraspinal tumours are presented. All were evaluated according to their ages, sex, signs and symptoms. The patients also had radiological and histopathological studies; and the ...
    • Successful Bone Marrow Transplantation in a Case Of Griscelli Disease which Presented in Accelerated Phase with Neurological Involvement 

      Tezcan, I; Sanal, O; Ersoy, F; Uckan, D; Kilic, S; Metin, A; Cetin, M; Akun, R; Oner, C; Tuncer, AM (Stockton Press, 1999)
      Griscelli disease (GD) is a rare disorder characterized by pigment dilution, immunodeficiency and occurrence of accelerated phase consisting of hemophagocytosis, pancytopenia and neurological manifestations, Allogeneic BMT ...