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Items: 1 to 20 of 89

1.
2.

A new nonrandom unbalanced t(17;20) in myeloid malignancies.

Patsouris C, Michael PM, Campbell LJ.

Cancer Genet Cytogenet. 2002 Oct 1;138(1):32-7.

PMID:
12419582
3.

Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.

Matteucci C, La Starza R, Crescenzi B, Romoli S, Santoro A, Magrin S, Lauria F, Coco FL, Martelli MF, Mecucci C.

Cancer Genet Cytogenet. 2003 Jan 1;140(1):13-7.

PMID:
12550752
4.

Deletion of chromosome 20q associated with hypereosinophilic syndrome. A report of two cases.

Brigaudeau C, Liozon E, Bernard P, Trimoreau F, Bordessoule D, Praloran V.

Cancer Genet Cytogenet. 1996 Mar;87(1):82-4.

PMID:
8646749
5.

[Abnormal karyotype, t(9;13)(q34;q12) in a patient with acute myelocytic leukemia].

Sato Y, Yoda Y, Kobayashi T, Tomiyama J, Abe T, Kondo I.

Rinsho Ketsueki. 1988 Nov;29(11):2163-7. Japanese. No abstract available.

PMID:
3236423
6.

Long-arm deletions in chromosome 6 in acute myelogenous leukemia: update on two cases.

Sundareshan TS, Lakshmi Devi V, Madhumathi DS, Appaji L, Girish MH, Prabhash K, Bapsy PP.

Cancer Genet Cytogenet. 2004 Oct 1;154(1):93-5. No abstract available.

PMID:
15381383
7.

Deletion of chromosome arm 15q in a case of minimally differentiated hypoplastic AML-M0.

Fujieda A, Masuya M, Kitano S, Miyazaki K, Yazaki A, Sugimoto Y, Usui E, Miyata E, Shibasaki T, Yamamura K, Ohishi K, Nishii K, Nakase K, Takeuchi T, Katayama N.

Cancer Genet Cytogenet. 2008 Jul;184(1):57-61. doi: 10.1016/j.cancergencyto.2008.03.010.

PMID:
18558291
8.
9.

Deletion 15q as the sole abnormality in acute myeloid leukemia: report of three cases and review of the literature.

Lu G, Yin CC, Medeiros LJ, Abruzzo LV.

Cancer Genet Cytogenet. 2009 Jan 15;188(2):118-23. doi: 10.1016/j.cancergencyto.2008.09.006. Review.

PMID:
19100517
10.

Prognostic significance of del(20q) in patients with hematological malignancies.

Brezinová J, Zemanová Z, Ransdorfová S, Sindelárová L, Sisková M, Neuwirtová R, Cermák J, Michalová K.

Cancer Genet Cytogenet. 2005 Jul 15;160(2):188-92.

PMID:
15993278
11.

Submicroscopic deletions in 5q- associated malignancies.

Crescenzi B, La Starza R, Romoli S, Beacci D, Matteucci C, Barba G, Aventin A, Marynen P, Ciolli S, Nozzoli C, Martelli MF, Mecucci C.

Haematologica. 2004 Mar;89(3):281-5.

12.

High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21.

Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Lai JL, Dastugue N, Macintyre E, Denis C, Bauters F, Kerckaert JP, Cosson A, Fenaux P.

Blood. 2000 Oct 15;96(8):2862-9.

13.

[Clinical and molecular cytogenetic features of myeloid diseases characterized by i(20q-): a study of seven cases].

Li TY, Xue YQ, Wu YF, Pan JL, Liu DD, Gong SL.

Zhonghua Yi Xue Za Zhi. 2004 May 2;84(9):732-5. Chinese.

PMID:
15200909
14.

Spontaneous complete remission of acute myeloid leukaemia with interstitial deletion of chromosome 5.

Narayanan MN, Lewis MJ.

Clin Lab Haematol. 1991;13(4):391-5. No abstract available.

PMID:
1773595
15.

Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia.

Shah N, Leaker MT, Teshima I, Baruchel S, Abdelhaleem M, Ye CC.

Pediatr Blood Cancer. 2008 May;50(5):1052-3. doi: 10.1002/pbc.21317.

PMID:
18213712
16.

MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).

Nilsson T, Nilsson L, Lenhoff S, Rylander L, Astrand-Grundström I, Strömbeck B, Höglund M, Turesson I, Westin J, Mitelman F, Jacobsen SE, Johansson B.

Genes Chromosomes Cancer. 2004 Nov;41(3):223-31.

PMID:
15334545
17.

Prognostic factors in adult patients up to 60 years old with acute myeloid leukemia and translocations of chromosome band 11q23: individual patient data-based meta-analysis of the German Acute Myeloid Leukemia Intergroup.

Krauter J, Wagner K, Schäfer I, Marschalek R, Meyer C, Heil G, Schaich M, Ehninger G, Niederwieser D, Krahl R, Büchner T, Sauerland C, Schlegelberger B, Döhner K, Döhner H, Schlenk RF, Ganser A.

J Clin Oncol. 2009 Jun 20;27(18):3000-6. doi: 10.1200/JCO.2008.16.7981. Epub 2009 Apr 20.

PMID:
19380453
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 15;156(2):154-7.

PMID:
15642396
19.

Isodicentric 7p, idic(7)(q11.2), in acute myeloid leukemia associated with older age and favorable response to induction chemotherapy: a new clinical entity?

Johansson B, Axelsson P, Billström R, Strömbeck B, Arheden K, Olofsson T, Cervin A, Adriansson M, Tanke HJ, Mitelman F, Fioretos T.

Genes Chromosomes Cancer. 2001 Mar;30(3):261-6.

PMID:
11170283
20.

[The long-term persistence of cell clone 47,XX,+I(1Q) in a female patient with multiyear complete clinico-hematological remission of acute myeloid leukemia].

Kobzev IuN, Udovichenko AI, Aseeva EA, Domracheva EV, Zakharova AV, Diachenko LV, Kuchma IuM.

Ter Arkh. 1997;69(7):59-61. Review. Russian. No abstract available.

PMID:
9424763

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