120 related articles for article (PubMed ID: 7627946)
1. Acute lymphoblastic leukemia in a patient with familial derivative chromosome 4.
Sasser EW; Wiley JE; Daeschner C
Cancer Genet Cytogenet; 1995 Jul; 82(1):90-2. PubMed ID: 7627946
[No Abstract] [Full Text] [Related]
2. Clinical significance of chromosome abnormalities in childhood acute lymphoblastic leukemia in Japan.
Kobayashi H; Maseki N; Homma C; Sakurai M; Kaneko Y
Leukemia; 1994 Nov; 8(11):1944-50. PubMed ID: 7967740
[TBL] [Abstract][Full Text] [Related]
3. [Applications of fluorescence in situ hybridization (FISH) in acute lymphoblastic leukemia].
Buades JM; Vizcarra Rabadán E; Sánchez Izquierdo D; Martínez-Climent JA
Sangre (Barc); 1999 Aug; 44(4):273-81. PubMed ID: 10589279
[No Abstract] [Full Text] [Related]
4. Detection of recurrent cytogenetic abnormalities in acute lymphoblastic and myeloid leukemias using fluorescence in situ hybridization.
Vance GH
Methods Mol Biol; 2013; 999():79-91. PubMed ID: 23666691
[TBL] [Abstract][Full Text] [Related]
5. Acute lymphoblastic leukemia with a novel t(3;12)(p25;q13).
Brozek I; Babińska M; Kuziemska E; Mrózek K; Limon J; Czyz J; Hellmann A
Cancer Genet Cytogenet; 1997 Sep; 97(2):167-8. PubMed ID: 9283603
[No Abstract] [Full Text] [Related]
6. Acute lymphoblastic leukemia with the 4;11 translocation exhibiting early T cell features.
Lo Coco F; Francia di Celle P; Alimena G; De Rossi G; Gastaldi R; Casorati G; Saglio G; Foa R
Leukemia; 1989 Jan; 3(1):79-82. PubMed ID: 2783347
[TBL] [Abstract][Full Text] [Related]
7. Chromosome 5 abnormalities in acute lymphoblastic leukemia.
Palau F; Prieto F; Badia L; Beneyto M; Benet I
Cancer Genet Cytogenet; 1991 Apr; 52(2):173-9. PubMed ID: 2021919
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
9. Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia.
Sharma P; Jarvis A; Jauch A; St Heaps L; Shaw P; Smith A
Cancer Genet Cytogenet; 2001 Jun; 127(2):177-80. PubMed ID: 11425460
[TBL] [Abstract][Full Text] [Related]
10. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
Alter D; Mark HF
Exp Mol Pathol; 2000 Oct; 69(2):152-8. PubMed ID: 11001863
[TBL] [Abstract][Full Text] [Related]
11. Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.
Tirado CA; Meloni-Ehrig AM; Edwards T; Scheerle J; Burks K; Repetti C; Christacos NC; Kelly JC; Greenberg J; Murphy C; Croft CD; Heritage D; Mowrey PN
Cancer Genet Cytogenet; 2007 Apr; 174(2):166-9. PubMed ID: 17452260
[TBL] [Abstract][Full Text] [Related]
12. Double isochromosome 8q as single cytogenetic aberration in acute myelo-monocytic leukemia.
Vicari L; Sebastio L; Cirigliano V; Pugliese MT; Ferrara F
Leuk Lymphoma; 1995 Oct; 19(3-4):351-3. PubMed ID: 8535230
[TBL] [Abstract][Full Text] [Related]
13. Unusual translocations and other changes in acute leukemia.
Ferro MT; del Potro E; Krsnik I; Villegas A; Fernández-Rañada JM; Resino M; García-Sagredo JM; San-Román C
Cancer Genet Cytogenet; 1991 Jul; 54(2):163-71. PubMed ID: 1884348
[TBL] [Abstract][Full Text] [Related]
14. [Detection of aberrant chromosomes in acute lymphoblastic leukemia by fluorescence in situ hybridization].
Yang K; Huang L
Zhonghua Xue Ye Xue Za Zhi; 1999 Dec; 20(12):640-2. PubMed ID: 11721367
[TBL] [Abstract][Full Text] [Related]
15. Three-way translocation involving band 6q21 in an acute lymphoblastic leukemia.
Berger R
Cancer Genet Cytogenet; 2007 Apr; 174(1):74-5. PubMed ID: 17350471
[No Abstract] [Full Text] [Related]
16. 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; 122(2):83-6. PubMed ID: 11106816
[TBL] [Abstract][Full Text] [Related]
17. Characterization of chromosomal breakpoints in an ALL patient using cross-species color banding.
Koo SH; Kwon KC; Park JW; Lee YE; Kim JW
Cancer Genet Cytogenet; 2000 Jun; 119(2):118-20. PubMed ID: 10867146
[TBL] [Abstract][Full Text] [Related]
18. Translocation t(1;10) (q21;q26) in a case of acute nonlymphocytic leukemia.
Terreros MC; Quesada M; Slavutsky IR
Acta Haematol; 1998; 99(2):92-4. PubMed ID: 9554457
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 22360868
[TBL] [Abstract][Full Text] [Related]
20. Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia case.
Wlodarska I; Baens M; Peeters P; Aerssens J; Mecucci C; Brock P; Marynen P; Van den Berghe H
Cancer Res; 1996 Jun; 56(11):2655-61. PubMed ID: 8653712
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
