126 related articles for article (PubMed ID: 12472589)
1. Does isochromosome 7q mandate bone marrow transplant in children with Shwachman-Diamond syndrome?
Cunningham J; Sales M; Pearce A; Howard J; Stallings R; Telford N; Wilkie R; Huntly B; Thomas A; O'Marcaigh A; Will A; Pratt N
Br J Haematol; 2002 Dec; 119(4):1062-9. PubMed ID: 12472589
[TBL] [Abstract][Full Text] [Related]
2. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Maserati E; Pressato B; Valli R; Minelli A; Sainati L; Patitucci F; Marletta C; Mastronuzzi A; Poli F; Lo Curto F; Locatelli F; Danesino C; Pasquali F
Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
[TBL] [Abstract][Full Text] [Related]
3. Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome.
Dror Y; Squire J; Durie P; Freedman MH
Leukemia; 1998 Oct; 12(10):1591-5. PubMed ID: 9766504
[TBL] [Abstract][Full Text] [Related]
4. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Sokolic RA; Ferguson W; Mark HF
Cancer Genet Cytogenet; 1999 Dec; 115(2):106-13. PubMed ID: 10598142
[TBL] [Abstract][Full Text] [Related]
5. SBDS mutations and isochromosome 7q in a patient with Shwachman-Diamond syndrome: no predisposition to malignant transformation?
Mellink CH; Alders M; van der Lelie H; Hennekam RH; Kuijpers TW
Cancer Genet Cytogenet; 2004 Oct; 154(2):144-9. PubMed ID: 15474150
[TBL] [Abstract][Full Text] [Related]
6. The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
Minelli A; Maserati E; Nicolis E; Zecca M; Sainati L; Longoni D; Lo Curto F; Menna G; Poli F; De Paoli E; Cipolli M; Locatelli F; Pasquali F; Danesino C
Leukemia; 2009 Apr; 23(4):708-11. PubMed ID: 19148133
[TBL] [Abstract][Full Text] [Related]
7. Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Maserati E; Minelli A; Olivieri C; Bonvini L; Marchi A; Bozzola M; Danesino C; Scappaticci S; Pasquali F
Cancer Genet Cytogenet; 2000 Sep; 121(2):167-71. PubMed ID: 11063802
[TBL] [Abstract][Full Text] [Related]
8. Monitoring the isochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR.
Porta G; Mattarucchi E; Maserati E; Pressato B; Valli R; Morerio C; Zecca M; Panarello C; Locatelli F; Lo Curto F; Pasquali F
J Pediatr Hematol Oncol; 2007 Mar; 29(3):163-5. PubMed ID: 17356395
[TBL] [Abstract][Full Text] [Related]
9. Isochromosome 7q in childhood myelodysplastic syndrome.
Murray JC; Mahoney DH; Cooley LD
Leukemia; 1996 Apr; 10(4):746-7. PubMed ID: 8618458
[No Abstract] [Full Text] [Related]
10. Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cells.
Ruiz-Gutierrez M; Bölükbaşı ÖV; Alexe G; Kotini AG; Ballotti K; Joyce CE; Russell DW; Stegmaier K; Myers K; Novina CD; Papapetrou EP; Shimamura A
JCI Insight; 2019 Apr; 5(12):. PubMed ID: 31039138
[TBL] [Abstract][Full Text] [Related]
11. Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome.
Smith A; Shaw PJ; Webster B; Lammi A; Gaskin K; Diaz S; Sharma P
Pediatr Hematol Oncol; 2002; 19(7):525-8. PubMed ID: 12217199
[TBL] [Abstract][Full Text] [Related]
12. Transient myelodysplastic syndrome associated with isochromosome 7q abnormality.
Leung EW; Woodman RC; Roland B; Abdelhaleem M; Freedman MH; Dror Y
Pediatr Hematol Oncol; 2003; 20(7):539-45. PubMed ID: 12959859
[TBL] [Abstract][Full Text] [Related]
13. Fluorescence in situ hybridization study of chromosome 7 aberrations in hepatosplenic T-cell lymphoma: isochromosome 7q as a common abnormality accumulating in forms with features of cytologic progression.
Wlodarska I; Martin-Garcia N; Achten R; De Wolf-Peeters C; Pauwels P; Tulliez M; de Mascarel A; Brière J; Patey M; Hagemeijer A; Gaulard P
Genes Chromosomes Cancer; 2002 Mar; 33(3):243-51. PubMed ID: 11807981
[TBL] [Abstract][Full Text] [Related]
14. Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.
Park TS; Song J; Lee JH; Kim JS; Yang WI; Choi JR
Ann Clin Lab Sci; 2009; 39(2):176-81. PubMed ID: 19429805
[TBL] [Abstract][Full Text] [Related]
15. Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Maserati E; Minelli A; Pressato B; Valli R; Crescenzi B; Stefanelli M; Menna G; Sainati L; Poli F; Panarello C; Zecca M; Curto FL; Mecucci C; Danesino C; Pasquali F
Genes Chromosomes Cancer; 2006 Apr; 45(4):375-82. PubMed ID: 16382447
[TBL] [Abstract][Full Text] [Related]
16. Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis?
Göhring G; Karow A; Steinemann D; Wilkens L; Lichter P; Zeidler C; Niemeyer C; Welte K; Schlegelberger B
Ann Hematol; 2007 Oct; 86(10):733-9. PubMed ID: 17653548
[TBL] [Abstract][Full Text] [Related]
17. Allogeneic stem cell transplantation for patients with acute myeloid leukemia or myelodysplastic syndrome who have chromosome 5 and/or 7 abnormalities.
van der Straaten HM; van Biezen A; Brand R; Schattenberg AV; Egeler RM; Barge RM; Cornelissen JJ; Schouten HC; Ossenkoppele GJ; Verdonck LF;
Haematologica; 2005 Oct; 90(10):1339-45. PubMed ID: 16219570
[TBL] [Abstract][Full Text] [Related]
18. Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes.
Saunders K; Czepulkowski B; Sivalingam R; Hayes JP; Aldouri M; Sekhar M; Cummins M; Ho A; Mufti GJ
Cancer Genet Cytogenet; 2005 Jan; 156(2):154-7. PubMed ID: 15642396
[TBL] [Abstract][Full Text] [Related]
19. Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome.
Pressato B; Marletta C; Montalbano G; Valli R; Maserati E
Br J Haematol; 2010 Sep; 150(5):632-3. PubMed ID: 20718726
[No Abstract] [Full Text] [Related]
20. Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia.
Mehta PA; Harris RE; Davies SM; Kim MO; Mueller R; Lampkin B; Mo J; Myers K; Smolarek TA
Cancer Genet Cytogenet; 2010 Dec; 203(2):180-6. PubMed ID: 21156231
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]