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Journal Abstract Search
142 related items for PubMed ID: 12377410
1. A novel t(16;20)(q22;p13) in polycythemia vera. Daibata M, Taguchi T, Taguchi H. Cancer Genet Cytogenet; 2002 Aug; 137(1):29-32. PubMed ID: 12377410 [Abstract] [Full Text] [Related]
2. Cryptic translocations involving chromosome 20 in polycythemia vera. Busson M, Romana S, Nguyen Khac F, Bernard O, Berger R. Ann Genet; 2004 Aug; 47(4):365-71. PubMed ID: 15581834 [Abstract] [Full Text] [Related]
3. HMGA2 overexpression in polycythemia vera with t(12;21)(q14;q22). Aliano S, Cirmena G, Garuti A, Fugazza G, Bruzzone R, Rocco I, Malacarne M, Ballestrero A, Sessarego M. Cancer Genet Cytogenet; 2007 Sep; 177(2):115-9. PubMed ID: 17854665 [Abstract] [Full Text] [Related]
4. Translocation (1;20)(q32;q13.3) in myelofibrosis following polycythemia vera. Davidovitz Y, Lev D, Ballin A, Tsudik A, Meytes D. Cancer Genet Cytogenet; 1998 Mar; 101(2):156-8. PubMed ID: 9494620 [Abstract] [Full Text] [Related]
5. Translocation t(3;21)(q26;q22) in acute myeloblastic leukemia secondary to polycythemia vera. Dastugue N, Pris J, Colombies P. Cancer Genet Cytogenet; 1990 Feb; 44(2):275-6. PubMed ID: 2297687 [Abstract] [Full Text] [Related]
6. A t(11;14)(p13;q11.2) in myelofibrosis following polycythemia vera. Jeong JH, Ahn JY, Park PW, Seo YH, Seo JY, Lee JH, Kim KH. Cancer Genet; 2016 Mar; 209(3):112-6. PubMed ID: 26826764 [Abstract] [Full Text] [Related]
14. der(1)t(1;9): a specific chromosome abnormality in polycythemia vera? Cytogenetic and in situ hybridization studies. den Nijs van Weert JI, Beverstock GC, Kievits T, Haak HL, Havik-Bogaard FC, Leeksma CH. Cancer Genet Cytogenet; 1989 Jul 01; 40(1):121-7. PubMed ID: 2758394 [Abstract] [Full Text] [Related]
15. t(8;21;8)(p23;q22;q22): a new variant form of t(8;21) translocation in acute myeloblastic leukemia with maturation. Xue Y, Xu L, Chen S, Fu J, Guo Y, Li J, Wu Y, Pan J, Lu D. Leuk Lymphoma; 2001 Jul 01; 42(3):533-7. PubMed ID: 11699421 [Abstract] [Full Text] [Related]
16. Fluorescence in situ hybridization identifies cryptic t(16;16)(p13;q22) masked by del(16)(q22) in a case of AML-M4 Eo. Merchant SH, Haines S, Hall B, Hozier J, Viswanatha DS. J Mol Diagn; 2004 Aug 01; 6(3):271-4. PubMed ID: 15269306 [Abstract] [Full Text] [Related]
17. Translocation (11;19)(q23;p13.3) associated with a novel t(5;16) (q13;q22) in a patient with acute myelocytic leukemia. Vendrame-Goloni CB, Varella-Garcia M, Carvalho-Salles AB, Ruiz MA, Júnior OR, Fett-Conte AC. Cancer Genet Cytogenet; 2003 Feb 01; 141(1):71-4. PubMed ID: 12581901 [Abstract] [Full Text] [Related]
18. Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders. Gray BA, Cornfield D, Bent-Williams A, Zori RT. Cancer Genet Cytogenet; 2003 Mar 01; 141(2):169-74. PubMed ID: 12606138 [Abstract] [Full Text] [Related]