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5. [Familial aplastic myelopathy (Fanconi's syndrome). Clinical contribution]. Pedone S; Corvaglia E; Vedovini F Atti Accad Fisiocrit Siena Med Fis; 1967; 16(2):1447-69. PubMed ID: 5621186 [No Abstract] [Full Text] [Related]
6. Fanconi familial hypoplastic anaemia. Mohammad T J Pak Med Assoc; 1981 Apr; 31(4):88-9. PubMed ID: 6785500 [No Abstract] [Full Text] [Related]
7. [Fanconi's anemia. Apropos of a case]. Pansera P; Pellicone M; Altomonte F; Carerj G; Carrabbotta F; Malaspina V; Fazzari C Minerva Pediatr; 1982 Mar; 34(5):229-39. PubMed ID: 7045627 [No Abstract] [Full Text] [Related]
8. Differentiation of Fanconi anemia from idiopathic aplastic anemia by induced chromosomal breakage study using mitomycin-C (MMC). Talwar R; Choudhry VP; Kucheria K Indian Pediatr; 2004 May; 41(5):473-7. PubMed ID: 15181297 [TBL] [Abstract][Full Text] [Related]
9. [Anemia due to anerythroblastosis (Blackfan-Diamond type) in a child with constitutional chromosomal abnormalities]. Brizard CP; Fayard C; Fraisse J; le Petit JC; Gannat B; Hermouet Y Pediatrie; 1971; 26(3):305-15. PubMed ID: 5557312 [No Abstract] [Full Text] [Related]
15. Spectrum of anomalies in Fanconi anaemia. Akar N; Gözdaşoğlu S J Med Genet; 1984 Feb; 21(1):75-6. PubMed ID: 6694193 [No Abstract] [Full Text] [Related]
16. [Prolonged exposure to ionizing radiation in a boy with aplastic anemia of Fanconi type]. Gumiński T; Strumińska J Przegl Lek; 1970 Sep; 26(9):724-5. PubMed ID: 5472565 [No Abstract] [Full Text] [Related]
17. [Chromosomal studies in 6 cases of Blackfan-Diamond anemia]. Philippe N; Requin C; Germain D Pediatrie; 1971; 26(1):47-54. PubMed ID: 5573306 [No Abstract] [Full Text] [Related]
18. Fanconi's anemia with isolated growth hormone deficiency. Zachmann M; Illig R; Prader A J Pediatr; 1972 Jan; 80(1):159-60. PubMed ID: 5062795 [No Abstract] [Full Text] [Related]
19. Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia. Cervenka J; Arthur D; Yasis C Pediatrics; 1981 Jan; 67(1):119-27. PubMed ID: 7243420 [TBL] [Abstract][Full Text] [Related]
20. [Granulocyte function defects, chromosome anomalies and blood group chimerism in 2 sisters with familial aplastic anemia (Estren-Dameshek type)]. Ebell W; Wahn V; Gebauer HJ; Kuntz B; Arnoldussen G; Göbel U Klin Padiatr; 1983; 195(4):283-7. PubMed ID: 6620941 [No Abstract] [Full Text] [Related] [Next] [New Search]