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3. Fanconi Anaemia associated with café au lait spots: A rare case report. Qazi M; Khan BA; Kumar V; Amin M; Ateeque K J Pak Med Assoc; 2024 Aug; 74(8):1575-1577. PubMed ID: 39160743 [TBL] [Abstract][Full Text] [Related]
4. [Fanconi anemia syndrome as a predisposing factor for acquired bone marrow aplasia]. Bin-Nun A; Soddeck M; Dar H; Berant M Harefuah; 1993 May; 124(10):610-1, 668. PubMed ID: 8344606 [TBL] [Abstract][Full Text] [Related]
6. The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia. Gonzalez CH; Durkin-Stamm MV; Geimer NF; Shahidi NT; Schilling RF; Rubira F; Opitz JM Birth Defects Orig Artic Ser; 1977; 13(3B):31-8. PubMed ID: 890097 [TBL] [Abstract][Full Text] [Related]
7. Medulloblastoma as a first presentation of fanconi anemia. Tischkowitz MD; Chisholm J; Gaze M; Michalski A; Rosser EM J Pediatr Hematol Oncol; 2004 Jan; 26(1):52-5. PubMed ID: 14707715 [TBL] [Abstract][Full Text] [Related]
8. Incidence of Fanconi anemia in children with congenital thumb anomalies referred for diepoxybutane testing. Webb ML; Rosen H; Taghinia A; McCarty ER; Cerrato F; Upton J; Labow BI J Hand Surg Am; 2011 Jun; 36(6):1052-7. PubMed ID: 21514743 [TBL] [Abstract][Full Text] [Related]
9. The first case of Niikawa-Kuroki syndrome in Kazakhstan associated with café au lait spots. Al Mosawi AJ; Fewin L G Ital Dermatol Venereol; 2009 Oct; 144(5):613-5. PubMed ID: 19834439 [TBL] [Abstract][Full Text] [Related]
10. Fanconi anemia with cleft palate. Jurca A; Kinga K; Bembea M; Gug C; Jurca C Rev Med Chir Soc Med Nat Iasi; 2014; 118(4):1074-7. PubMed ID: 25581972 [TBL] [Abstract][Full Text] [Related]
11. [Two cases of cytopenia associated with multiple malformations]. Chang LX; Zhang L; Gao YM; Zhu XF Zhongguo Dang Dai Er Ke Za Zhi; 2024 Apr; 26(4):410-413. PubMed ID: 38660906 [TBL] [Abstract][Full Text] [Related]
12. [McCune-Albright syndrome revealed by Blaschko-linear café-au-lait spots on the back]. Jung AJ; Soskin S; Paris F; Lipsker D Ann Dermatol Venereol; 2016 Jan; 143(1):21-6. PubMed ID: 26610360 [TBL] [Abstract][Full Text] [Related]
13. [Constitutional aplastic pancytopenia in children (author's transl)]. Gluckman E; Devergie A Sem Hop; 1982 Feb; 58(7):423-6. PubMed ID: 6280317 [TBL] [Abstract][Full Text] [Related]
14. Multiple dysmorphic features and pancytopenia: a new syndrome? Sackey K; Sakati N; Aur RJ; Shebib S; Sabbah RS; Rifai S Clin Genet; 1985 Jun; 27(6):606-10. PubMed ID: 4017281 [TBL] [Abstract][Full Text] [Related]
15. Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry. Rosenberg PS; Alter BP; Ebell W Haematologica; 2008 Apr; 93(4):511-7. PubMed ID: 18322251 [TBL] [Abstract][Full Text] [Related]
16. New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia. Giampietro PF; Auerbach AD; Elias ER; Gutman A; Zellers NJ; Davis JG Am J Med Genet; 1998 Jun; 78(1):70-5. PubMed ID: 9637428 [TBL] [Abstract][Full Text] [Related]
17. A new autosomal recessive syndrome. Early onset of pancytopenia, distinct facial features, growth retardation and developmental delay. Al-Batniji FS; Mahmoud MA; Van Dijken PJ; Al-Asiri RH; Al-Swaid AF; Al-Marshedy AM Saudi Med J; 2001 Dec; 22(12):1122-6. PubMed ID: 11802189 [TBL] [Abstract][Full Text] [Related]
18. Bone marrow failure: a child is not just a small adult (but an adult can have a childhood disease). Alter BP Hematology Am Soc Hematol Educ Program; 2005; ():96-103. PubMed ID: 16304365 [TBL] [Abstract][Full Text] [Related]
20. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation. Mathieu M; De Broca A; Bony H; Piussan C Genet Couns; 1993; 4(4):299-303. PubMed ID: 8110419 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]