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Items: 1 to 20 of 117

1.

Philadelphia chromosome positive acute B-lymphoblastic leukemia with extreme leukocytosis.

Bhatnagar V, Emadi A.

Blood. 2013 Aug 15;122(7):1104. No abstract available.

2.

Variant intra philadelphia translocation with rearrangement of BCR-ABL and ABL-BCR within the same chromosome in a patient with cALL.

Edelhäuser M, Raber W, Mitterbauer G, Mannhalter C, Lechner K, Fonatsch C.

Cancer Genet Cytogenet. 2000 Oct 15;122(2):83-6.

PMID:
11106816
3.

Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization.

Cetin Z, Yakut S, Karadogan I, Kupesiz A, Timuragaoglu A, Salim O, Tezcan G, Alanoglu G, Ozbalci D, Hazar V, Yesilipek MA, Undar L, Luleci G, Berker S.

Genet Test Mol Biomarkers. 2012 May;16(5):318-23. doi: 10.1089/gtmb.2011.0186. Epub 2012 Feb 23.

PMID:
22360868
4.

Double fusion signal BCR/ABL, detected by FISH on chromosomes 9 and 22 in a child with ALL.

Jarosová M, Mihál V, Holzerová M, Jedlicková K, Pospisilová, Pikalová Z, Indrák K.

Leukemia. 2000 Jul;14(7):1319-22. No abstract available.

PMID:
10914561
5.

BCR/ABL fusion gene detected on 9q34 by fluorescence in situ hybridization in an acute leukemia with two BCR/ABL positive clones, one Ph-negative and one Ph-positive.

Terré C, Bastie JN, Garcia I, Suzan F, Cayuela JM, Therond P, Castaigne S.

Cancer Genet Cytogenet. 2001 Nov;131(1):37-41.

PMID:
11734316
6.

High prevalence of BCR-ABL fusion transcripts with poor prognostic impact among adult ALL patients: report from Pakistan.

Faiz M, Iqbal QJ, Qureshi A.

Asia Pac J Clin Oncol. 2011 Mar;7(1):47-55. doi: 10.1111/j.1743-7563.2010.01370.x. Epub 2011 Feb 14.

PMID:
21332651
7.

Complex chromosome rearrangements may locate the bcr/abl fusion gene sites other than 22q11.

Sessarego M, Fugazza G, Bruzzone R, Ballestrero A, Miglino M, Bacigalupo A.

Haematologica. 2000 Jan;85(1):35-9.

8.

BCR rearrangement without juxtaposition of ABL in pre-T acute lymphoblastic leukaemia.

Fosså A, Siebert R, Kasper C, Becher R, Opalka B, Thiel E, Seeber S, Nowrousian MR.

Br J Haematol. 1996 May;93(2):403-5.

PMID:
8639438
9.

Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome.

Durmaz B, Karaca E, Vural F, Cogulu O, Alpman A, Tombuloglu M, Ozkinay F.

Acta Oncol. 2008;47(8):1604-6. doi: 10.1080/02841860802078077. No abstract available.

PMID:
18607844
10.

Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridization.

Tosi S, Cabot G, Giudici G, Attuati V, Morandi P, Rambaldi A, Döhner H, Biondi A.

Cancer Genet Cytogenet. 1996 Jul 15;89(2):153-6.

PMID:
8697423
11.

Molecular diagnosis and clinical relevance of t(9;22), t(4;11) and t(1 ;19) chromosome abnormalities in a consecutive group of 141 adult patients with acute lymphoblastic leukemia.

Rambaldi A, Attuati V, Bassan R, Neonato MG, Viero P, Battista R, Di Bona E, Rossi G, Pogliani E, Ruggeri M, Amaru R, Rivolta A, Giudici G, Biondi A, Barbui T.

Leuk Lymphoma. 1996 May;21(5-6):457-66.

PMID:
9172811
12.

A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1).

Todorić-Zivanović B, Marisavljević D, Surace C, Cemerikić V, Marković O, Krtolica K, Tatomirović Z, Cikota B, Magić Z, Rocchi M.

Cancer Genet Cytogenet. 2006 Apr 15;166(2):180-5.

PMID:
16631477
13.

Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia.

Buijs A, Terhal PA, Thunnissen PL.

Cancer Genet Cytogenet. 2006 Jul 1;168(1):80-2. No abstract available.

PMID:
16772126
14.
15.

Application of fluorescence in situ hybridization in defining a complex t(9;21;22) Ph formation.

Mancini M, Nanni M, Cedrone M, De Cuia MR, Rondinelli MB, Malagnino F, Alimena G.

Haematologica. 1994 Nov-Dec;79(6):536-9.

16.
17.

Expression of CD25 is a specific and relatively sensitive marker for the Philadelphia chromosome (BCR-ABL1) translocation in pediatric B acute lymphoblastic leukemia.

Gaikwad AS, Donohue RE, Elghetany MT, Sheehan AM, Lu XY, Gramatges MM, McClain KL, Mistretta TA, Punia JN, Moore TJ, Goltsova T, Cubbage M, Curry CV.

Int J Clin Exp Pathol. 2014 Aug 15;7(9):6225-30. eCollection 2014.

18.

Patterns of BCR/ABL gene rearrangements by interphase fluorescence in situ hybridization (FISH) in BCR/ABL+ leukemias: incidence and underlying genetic abnormalities.

Primo D, Tabernero MD, Rasillo A, Sayagués JM, Espinosa AB, Chillón MC, Garcia-Sanz R, Gutierrez N, Giralt M, Hagemeijer A, San Miguel JF, Orfao A.

Leukemia. 2003 Jun;17(6):1124-9.

PMID:
12764379
19.

Leading prognostic relevance of the BCR-ABL translocation in adult acute B-lineage lymphoblastic leukemia: a prospective study of the German Multicenter Trial Group and confirmed polymerase chain reaction analysis.

Gleissner B, Gökbuget N, Bartram CR, Janssen B, Rieder H, Janssen JW, Fonatsch C, Heyll A, Voliotis D, Beck J, Lipp T, Munzert G, Maurer J, Hoelzer D, Thiel E; German Multicenter Trials of Adult Acute Lymphoblastic Leukemia Study Group.

Blood. 2002 Mar 1;99(5):1536-43.

20.

Philadelphia-positive acute lymphoblastic leukemia with multiple subclones including duplication of the Philadelphia chromosome and Abelson oncogene.

La Starza R, Vitale A, Serra A, Saglio G, Fioritoni G, Falzetti D, Martelli MF, Foà R, Mecucci C.

Cancer Genet Cytogenet. 2002 Jan 1;132(1):46-50.

PMID:
11801308
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