127 related articles for article (PubMed ID: 7987809)
1. Chromosome derived from translocation(1;17) retains alphoid sequences of both chromosomes involved.
Fugazza G; Bruzzone R; Sessarego M
Cancer Genet Cytogenet; 1994 Nov; 78(1):7-9. PubMed ID: 7987809
[TBL] [Abstract][Full Text] [Related]
2. Unbalanced 1q whole-arm translocation resulting in der(14)t(1;14)(q11-12;p11) in myelodysplastic syndrome.
Fogu G; Campus PM; Cambosu F; Moro MA; Sanna R; Fozza C; Nieddu RM; Longinotti M; Montella A
Cytogenet Genome Res; 2012; 136(4):256-63. PubMed ID: 22571950
[TBL] [Abstract][Full Text] [Related]
3. Complex structural involvement of chromosome 7 in primary myelodysplastic syndromes determined by fluorescence in situ hybridization.
Sessarego M; Fugazza G; Gobbi M; Bruzzone R; Bisio R; Ghio R; Patrone F
Cancer Genet Cytogenet; 1998 Oct; 106(2):110-5. PubMed ID: 9797774
[TBL] [Abstract][Full Text] [Related]
4. Confirmation of centromeric fusion in 7p/1q translocation associated with myelodysplastic syndrome.
Hoo JJ; Szego K; Jones B
Cancer Genet Cytogenet; 1992 Dec; 64(2):186-8. PubMed ID: 1486571
[TBL] [Abstract][Full Text] [Related]
5. Translocation t(1;17)(q12;q25) with a clinical picture like of a proximal deletion of 1q: identification by in situ hybridization with chromosome 1-specific satellite DNA probes.
Vorsanova SG; Yurov YB; Kurbatov MB; Kazantzeva LZ
Hum Genet; 1990 Dec; 86(2):173-4. PubMed ID: 2265830
[TBL] [Abstract][Full Text] [Related]
6. Hyperdiploid karyotype in a childhood MDS patient.
Acar H; Calişkan U U; Kaynak M; Yildirim MS; Largaespada DA
Clin Lab Haematol; 2001 Aug; 23(4):255-8. PubMed ID: 11683788
[TBL] [Abstract][Full Text] [Related]
7. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
[TBL] [Abstract][Full Text] [Related]
9. Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.
Parada LA; Limon J; Iliszko M; Czauderna P; Gisselsson D; Höglund M; Kullendorff CM; Wiebe T; Mertens F; Johansson B
Med Pediatr Oncol; 2000 Mar; 34(3):165-70. PubMed ID: 10696121
[TBL] [Abstract][Full Text] [Related]
10. Translocation t(6;9)(p22.3;q34) in myelodysplastic syndrome--refractory anemia with excess blasts.
Fan YS; Raza A; Schumer J; Sait SN; Block AW; Snyderman M; Sandberg AA
Cancer Genet Cytogenet; 1987 Nov; 29(1):135-8. PubMed ID: 3664444
[TBL] [Abstract][Full Text] [Related]
11. Identification of cytogenetically undetected 12p13 translocations and associated deletions with fluorescence in situ hybridization.
Kobayashi H; Rowley JD
Genes Chromosomes Cancer; 1995 Jan; 12(1):66-9. PubMed ID: 7534114
[TBL] [Abstract][Full Text] [Related]
12. Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH).
Han K; Lee W; Harris CP; Kim W; Shim S; Meisner LF
Leukemia; 1994 Jan; 8(1):81-6. PubMed ID: 8289503
[TBL] [Abstract][Full Text] [Related]
13. Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization.
Gravholt CH; Friedrich U; Caprani M; Jørgensen AL
Genomics; 1992 Dec; 14(4):924-30. PubMed ID: 1478673
[TBL] [Abstract][Full Text] [Related]
14. Duplication of one of the products of the t(8;21) translocation in a patient with refractory anemia with excess blasts in transformation.
Czepulkowski B; Gibbons B; Tucker J; Amess J; Lister TA
Cancer Genet Cytogenet; 1987 Mar; 25(1):175-7. PubMed ID: 3802052
[TBL] [Abstract][Full Text] [Related]
15. Combined trisomy 1q and monosomy 17p due to translocation t(1;17) in a patient with myelodysplastic syndrome.
Mamaev N; Mamaeva SE; Pavlova VA; Patterson D
Cancer Genet Cytogenet; 1988 Oct; 35(1):21-5. PubMed ID: 3180004
[TBL] [Abstract][Full Text] [Related]
16. Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts (RAEB).
Calabrese G; Fantasia D; Morizio E; Toro PM; Franchi PG; Fornaro A; Spadano A; Stuppia L; Palka G
Br J Haematol; 2003 Sep; 122(5):760-3. PubMed ID: 12930385
[TBL] [Abstract][Full Text] [Related]
17. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
Perfumo C; Arslanian A; Zara F; Piombo G; Pierluigi M
Pathologica; 1992; 84(1091):363-9. PubMed ID: 1465321
[TBL] [Abstract][Full Text] [Related]
18. [Dual-color FISH study on myelodysplastic syndrome with 1;7 translocation].
Shen Y; Xue Y; Li J; Pan J; Wu Y; Guo Y; Lu D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):313-6. PubMed ID: 12170469
[TBL] [Abstract][Full Text] [Related]
19. Two-color FISH characterization of i(1q) and der(1;16) in human breast cancer cells.
Kokalj-Vokac N; Alemeida A; Gerbault-Seureau M; Malfoy B; Dutrillaux B
Genes Chromosomes Cancer; 1993 May; 7(1):8-14. PubMed ID: 7688559
[TBL] [Abstract][Full Text] [Related]
20. 17q21-qter trisomy is an indicator of poor prognosis in acute myelogenous leukemia.
Morerio C; Russo I; Rosanda C; Rapella A; Leszl A; Basso G; Maserati E; Pasquali F; Panarello C
Cancer Genet Cytogenet; 2001 Jan; 124(1):12-5. PubMed ID: 11165316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]