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2. Clonal evolution in a transforming 5q- syndrome. Kandioler D; Krieger O; Nowotny H; Lutz D Leukemia; 1994 Apr; 8(4):711-2. PubMed ID: 8152269 [No Abstract] [Full Text] [Related]
3. [5q anomaly in myelodysplasia and acute myelocytic leukemia]. Robak T Acta Haematol Pol; 1990; 21(2):235-42. PubMed ID: 2151871 [No Abstract] [Full Text] [Related]
4. Assignment of the GM-CSF, CSF-1, and FMS genes to human chromosome 5 provides evidence for linkage of a family of genes regulating hematopoiesis and for their involvement in the deletion (5q) in myeloid disorders. Le Beau MM; Pettenati MJ; Lemons RS; Diaz MO; Westbrook CA; Larson RA; Sherr CJ; Rowley JD Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 2():899-909. PubMed ID: 3495397 [No Abstract] [Full Text] [Related]
5. [Refractory anemia with 5q--anomaly. Clinical picture and follow-up of seven patients]. May D; Becher R Med Klin (Munich); 1992 Aug; 87(8):408-11. PubMed ID: 1406472 [TBL] [Abstract][Full Text] [Related]
7. The 5q- syndrome. Van den Berghe H Scand J Haematol Suppl; 1986; 45():78-81. PubMed ID: 3457446 [No Abstract] [Full Text] [Related]
8. Assignment of CSF-1 to 5q33.1: evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders. Pettenati MJ; Le Beau MM; Lemons RS; Shima EA; Kawasaki ES; Larson RA; Sherr CJ; Diaz MO; Rowley JD Proc Natl Acad Sci U S A; 1987 May; 84(9):2970-4. PubMed ID: 3495006 [TBL] [Abstract][Full Text] [Related]
9. Late appearing 5q--marker in refractory anemia. Heim S; Billström R; Kristoffersson U; Mandahl N; Mitelman F Cancer Genet Cytogenet; 1987 Jan; 24(1):159-62. PubMed ID: 3466668 [TBL] [Abstract][Full Text] [Related]
11. Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders. Le Beau MM; Westbrook CA; Diaz MO; Larson RA; Rowley JD; Gasson JC; Golde DW; Sherr CJ Science; 1986 Feb; 231(4741):984-7. PubMed ID: 3484837 [TBL] [Abstract][Full Text] [Related]
12. [Constitutional pericentric inversions of chromosomes 5, 7 and 9 in patients with myeloid tumors]. Ol'shanskaia IuV; Udovichenko AI; Vodinskaia LA; Savchenko VG; Domracheva EV Ter Arkh; 2001; 73(7):68-70. PubMed ID: 11523415 [No Abstract] [Full Text] [Related]
13. Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint. Boultwood J; Fidler C; Lewis S; Kelly S; Sheridan H; Littlewood TJ; Buckle VJ; Wainscoat JS Genomics; 1994 Feb; 19(3):425-32. PubMed ID: 8188284 [TBL] [Abstract][Full Text] [Related]
14. Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome. Pellagatti A; Cazzola M; Giagounidis A; Perry J; Malcovati L; Della Porta MG; Jädersten M; Killick S; Vyas P; Hellström-Lindberg E; Wainscoat JS; Boultwood J Br J Haematol; 2011 Oct; 155(2):272-4. PubMed ID: 21492127 [No Abstract] [Full Text] [Related]
15. Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q. Gao Q; Horwitz M; Roulston D; Hagos F; Zhao N; Freireich EJ; Golomb HM; Olopade OI Genes Chromosomes Cancer; 2000 Jun; 28(2):164-72. PubMed ID: 10825001 [TBL] [Abstract][Full Text] [Related]
16. [Chromosome 5q deletion in a patient with persistant anemia which subsequently developed into acute non-differentiated leukemia]. Cabrol C; Abele R Arch Genet (Zur); 1978; 51(2):53-5. PubMed ID: 757124 [No Abstract] [Full Text] [Related]
17. Dihydrofolate reductase activity in the erythroblasts of patients with 5q- syndrome. Nano R; Invernizzi R; Pecci A; Civallero M; Gerzeli G Haematologica; 2000 Jul; 85(7):765-6. PubMed ID: 10897132 [No Abstract] [Full Text] [Related]
19. 5q- syndrome in a child. Uyttebroeck A; Brock P; De Groote B; Renard M; Dal Cin P; Van den Berghe H; Casteels-Van Daele M Cancer Genet Cytogenet; 1995 Apr; 80(2):121-3. PubMed ID: 7736428 [TBL] [Abstract][Full Text] [Related]
20. High resolution analysis of the 5q-marker chromosome in refractory anemia. Mitelman F; Manolova Y; Manolov G; Billström R; Heim S; Kristoffersson U; Mandahl N Hereditas; 1986; 105(1):49-54. PubMed ID: 3793519 [No Abstract] [Full Text] [Related] [Next] [New Search]