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Cytogenetics Database CytoD 1.0

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Query: inv(16)(p13q22)

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inv(16)(p13q22)     Molecular analysis of a new variant of the CBF beta-MYH11 gene fusion. Leuk Lymphoma. 2002 Oct;43(10):2021-6.
inv(16)(p13q22)     Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia. Leukemia. 1996 Sep;10(9):1459-62.
inv(16)(p13q22)     Myelodysplastic syndrome in children: differentiation from acute myeloid leukemia with a low blast count. Leukemia. 1997 Feb;11(2):206-11.
inv(16)(p13q22)     NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16). Eur J Haematol. 1996 Jan-Feb;56(1-2):68-71.
inv(16)(p13q22)     Nonrandom additional chromosome changes in acute nonlymphocytic leukemia with inv(16)(p13q22). Cancer Genet Cytogenet. 1987 Jun;26(2):309-15.
inv(16)(p13q22)     The significance of trisomy 8 in de novo acute myeloid leukaemia: the accompanying chromosome aberrations determine the prognosis. German AML Cooperative Study Group. Br J Haematol. 1997 Dec;99(3):605-11.
inv(16)(p13q22)     Granulocytic sarcoma with translocation (9;11)(p22;q23): two cases. Cancer Genet Cytogenet. 1997 Jul 15;96(2):115-7.
inv(16)(p13q22)     Comment in: Leukemia. 2003 Mar;17(3):650-1; author reply 651-2. Leukemia. 2002 Jun;16(6):1176-81.
inv(16)(p13q22)     Typical CBFbeta/MYH11 fusion due to insertion of the 3'-MYH11 gene into 16q22 in acute monocytic leukemia with normal chromosomes 16 and trisomies 8 and 22. Cancer Genet Cytogenet. 2000 Dec;123(2):137-9.
inv(16)(p13q22)     CBFB/MYH11 fusion transcripts in a case of acute myelogenous leukemia (M1) with partial deletion of the long arm of chromosome 16. Intern Med. 1996 Apr;35(4):327-30.
inv(16)(p13q22)     Trisomy 16 as the sole anomaly in hematological malignancies. Three new cases and a short review. Cancer Genet Cytogenet. 2001 Jul 15;128(2):168-71.
inv(16)(p13q22)     Secondary acute myeloid leukemia with inv(16): report of two cases following paclitaxel-containing chemotherapy and review of the role of intensified ara-C therapy. Leukemia. 1999 Nov;13(11):1735-40.
inv(16)(p13q22)     Abnormalities of chromosome 16 in association with acute myelomonocytic leukemia and dysplastic bone marrow eosinophils. J Clin Oncol. 1984 Jun;2(6):550-7.
inv(16)(p13q22)     The biological significance of the multidrug resistance gene MRP in inversion 16 leukemias. Leuk Lymphoma. 1996 Feb;20(5-6):357-64.
inv(16)(p13q22)     Acute myelomonocytic leukemia with inv(16)(p13q22) in an XY/XYY male. Cancer Genet Cytogenet. 1987 Dec;29(2):331-2.
inv(16)(p13q22)     Cytogenetic studies on acute myelomonocytic leukaemia (M4) with eosinophilia. Leuk Res. 1985;9(2):279-88.
inv(16)(p13q22)     Abnormalities of chromosome 16q in myeloid malignancy: 14 new cases and a review of the literature. Leukemia. 1992 Dec;6(12):1250-6.
inv(16)(p13q22)     Inversion of chromosome 16 and dysplastic eosinophils in accelerated phase of chronic myeloid leukemia. Leukemia. 1992 May;6(5):381-4.
inv(16)(p13q22)     Acquisition of additional primary chromosome abnormalities in the course of karyotype evolution in a case of FAB-M2 acute leukemia. Cancer Genet Cytogenet. 1989 Jul 1;40(1):105-10.
inv(16)(p13q22)     Philadelphia-positive acute myelomonocytic leukemia with inversion of chromosome 16 and eosinobasophils. Am J Hematol. 1988 Jan;27(1):69-71.
inv(16)(p13q22)     Karyotypic evolution in acute myelomonocytic leukemia with pericentric inversion of chromosome 16. Cancer Genet Cytogenet. 1987 Feb;24(2):257-62.
inv(16)(p13q22)     Heritable fragile sites and cancer: fra(16)(q22) in lymphocytes of an acute nonlymphocytic leukemia patient with inv(16)(p13q22). Cancer Genet Cytogenet. 1987 Mar;25(1):81-6.
inv(16)(p13q22)     Inversion of chromosome 16 with the Philadelphia chromosome in acute myelomonocytic leukemia with eosinophilia. Report of two cases. Cancer Genet Cytogenet. 1992 Jan;58(1):29-34.
inv(16)(p13q22)     Identification of a novel CBFB-MYH11 transcript: implications for RT-PCR diagnosis. Hematol J. 2001;2(3):206-9.
inv(16)(p13q22)     Pericentric inversion of chromosome 16 in a large kindred: spectrum of morbidity and mortality in offspring. Am J Med Genet. 1992 Jul 15;43(5):791-5.
inv(16)(p13q22)     Morphologic, immunologic, and cytogenetic classification of acute myeloid leukemia and myelodysplastic syndrome in childhood: a report from the Childrens Cancer Group. Leukemia. 1996 Jan;10(1):5-12.
inv(16)(p13q22)     Granulocytic sarcoma of the small intestine preceding acute myelomonocytic leukemia with abnormal eosinophils and inv(16). Cancer Genet Cytogenet. 1988 Oct 15;35(2):231-5.
inv(16)(p13q22)     Detection of minimal residual disease in acute myelomonocytic leukemia with abnormal marrow eosinophils by nested polymerase chain reaction with allele specific amplification. Blood. 1994 Oct 1;84(7):2291-6.
inv(16)(p13q22)     Acquired inversions in human leucocytes. Ann Genet. 1986;29(3):203-6.
inv(16)(p13q22)     Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia. Science. 1993 Aug 20;261(5124):1041-4.
inv(16)(p13q22)     Hypoplastic acute leukemia associated with inv(16)(p13q22). Cancer Genet Cytogenet. 1991 Jan;51(1):63-6.
inv(16)(p13q22)     Comparison of cytogenetic and molecular genetic detection of t(8;21) and inv(16) in a prospective series of adults with de novo acute myeloid leukemia: a Cancer and Leukemia Group B Study. J Clin Oncol. 2001 May 1;19(9):2482-92.
inv(16)(p13q22)     Acute myeloid leukemia M4 with bone marrow eosinophilia (M4Eo) and inv(16)(p13q22) exhibits a specific immunophenotype with CD2 expression. Blood. 1993 Jun 1;81(11):3043-51.
inv(16)(p13q22)     Detection of a dup(17q) and inv(16) by fluorescence in situ hybridization in acute myelomonocytic leukemia. Cancer Genet Cytogenet. 1997 Oct 1;98(1):87-9.
inv(16)(p13q22)     Chromosome 16 inversion-associated translocations in acute myeloid leukemia elucidated using a dual-color CBFB DNA probe. Cancer Genet Cytogenet. 2002 Apr 15;134(2):142-4.
inv(16)(p13q22)     Detection of inv(16)(p13q22) by means of chromosome painting with a 16q-specific probe. Cancer Genet Cytogenet. 2004 Apr 1;150(1):86-7.
inv(16)(p13q22)     Central nervous system involvement in acute nonlymphocytic leukemia with inv(16)(p13q22). Leukemia. 1988 Jun;2(6):398-9.
inv(16)(p13q22)     FISH identifies inv(16)(p13q22) masked by translocations in three cases of acute myeloid leukemia. Genes Chromosomes Cancer. 1998 Jun;22(2):87-94.
inv(16)(p13q22)     Core-binding factor: a central player in hematopoiesis and leukemia. Cancer Res. 1999 Apr 1;59(7 Suppl):1789s-1793s.
inv(16)(p13q22)     Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia. Cancer Genet Cytogenet. 1992 Mar;59(1):35-8.
inv(16)(p13q22)     Mechanism of leukemogenesis by the inv(16) chimeric gene CBFB/PEBP2B-MHY11. Oncogene. 2004 May 24;23(24):4297-307.
inv(16)(p13q22)     Multiple karyotypic aberrations in a polymorphous variant of Waldenström macroglobulinemia. Cancer Genet Cytogenet. 1999 May;111(1):77-80.
inv(16)(p13q22)     Acute myelomonocytic leukemia with bone marrow eosinophilia and inv(16)(p13q22),t(1;16)(q32;q22). Cancer Genet Cytogenet. 1991 Feb;51(2):235-8.
inv(16)(p13q22)     Childhood acute myeloid leukemia with CBFbeta-MYH11 rearrangement: study of incidence, morphology, cytogenetics, and clinical outcomes of Chinese in Hong Kong. Am J Hematol. 2004 Jul;76(3):300-3.
inv(16)(p13q22)     Comment in: Leuk Res. 1994 Dec;18(12):889-90. Leuk Res. 1994 Dec;18(12):885-8.
inv(16)(p13q22)     Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: a study of 90 patients. Br J Haematol. 2001 Jan;112(1):118-26.
inv(16)(p13q22)     Deletion of 16q11 is a recurrent cytogenetic aberration in acute myeloblastic leukemia during disease progression. Cancer Genet Cytogenet. 2001 Nov;131(1):65-8.
inv(16)(p13q22)     Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients. Blood. 1989 Oct;74(5):1781-90.
inv(16)(p13q22)     FISH mapping of a human chromosome 16 constitutional pericentric inversion inv(16)(p13q22) found in a large kindred. Am J Med Genet. 1994 Sep 1;52(3):346-8.
inv(16)(p13q22)     Comment in: Br J Haematol. 1995 Jul;90(3):732-3. Br J Haematol. 1995 Mar;89(3):531-4.
inv(16)(p13q22)     Chromosome studies on 30 Chinese patients with acute nonlymphocytic leukemia in Taiwan. Cancer Genet Cytogenet. 1988 May;32(1):101-8.
inv(16)(p13q22)     Standard Ph chromosome, t(9;22)(q34;q11), as an additional change in a patient with acute myelomonocytic leukemia (M4Eo) associated with inv(16)(p13q22) Am J Hematol. 1994 Jan;45(1):94-6.
inv(16)(p13q22)     A unique structural abnormality of chromosome 16 resulting in a CBF beta-MYH11 fusion transcript in a patient with acute myeloid leukemia, FAB M4. Cancer Genet Cytogenet. 2000 Aug;121(1):52-5.
inv(16)(p13q22)     Quantification of CBFbeta/MYH11 fusion transcript by real time RT-PCR in patients with INV(16) acute myeloid leukemia. Leukemia. 2001 Jul;15(7):1072-80.
inv(16)(p13q22)     Acute myeloid leukemia with inv(16)(p13q22): involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign. Am J Hematol. 2002 Sep;71(1):15-9.
inv(16)(p13q22)     RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB-MYH11 transcripts. Blood. 1995 Jul 1;86(1):277-82.
inv(16)(p13q22)     Cytogenetically cryptic AML1-ETO and CBF beta-MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia. Br J Haematol. 2000 Dec;111(4):1051-6.
inv(16)(p13q22)     Inversion of chromosome 16 and bone marrow eosinophilia in a myelomonocytic transformation of chronic myeloid leukemia. Cancer Genet Cytogenet. 1992 Jul 15;61(2):197-200.
inv(16)(p13q22)     A morphologic and cytochemical study of acute myelomonocytic leukemia with abnormal marrow eosinophils associated with inv(16)(p13q22). Am J Clin Pathol. 1984 Jun;81(6):733-41.
inv(16)(p13q22)     A unique pattern of central nervous system leukemia in acute myelomonocytic leukemia associated with inv(16)(p13q22). Blood. 1985 May;65(5):1071-8.
inv(16)(p13q22)     A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo. Blood. 1993 Nov 15;82(10):2948-52.
inv(16)(p13q22)     Chromosome change at 16q22 in nonlymphocytic leukemia: clinical implication on leukemia patients with inv(16) versus del(16). Leukemia. 1988 Jan;2(1):35-40.
inv(16)(p13q22)     Monosomy 16 as the sole abnormality in myeloid malignancies. Cancer Genet Cytogenet. 2000 Apr 15;118(2):163-6.
inv(16)(p13q22)     Frequency of CBF beta/MYH11 fusion transcripts in patients entered into the U.K. MRC AML trials. The MRC Adult Leukaemia Working Party. Br J Haematol. 1997 Mar;96(4):736-9.
inv(16)(p13q22)     Repetitive cycles of high-dose cytarabine benefit patients with acute myeloid leukemia and inv(16)(p13q22) or t(16;16)(p13;q22): results from CALGB 8461. J Clin Oncol. 2004 Mar 15;22(6):1087-94.
inv(16)(p13q22)     Two-colour FISH detection of the inv(16) in interphase nuclei of patients with acute myeloid leukaemia. Br J Haematol. 1999 Jul;106(1):111-4.
inv(16)(p13q22)     Dysplasia and high proliferation rate are common in acute myeloid leukemia with inv(16)(p13q22). Am J Clin Pathol. 2003 Aug;120(2):236-45.
inv(16)(p13q22)     Inversion of chromosome 16 and uncommon rearrangements of the CBFB and MYH11 genes in therapy-related acute myeloid leukemia: rare events related to DNA-topoisomerase II inhibitors? J Clin Oncol. 1998 May;16(5):1890-6.
inv(16)(p13q22)     Three cases of the myelodysplastic syndrome with pericentric inversion of chromosome 16. Br J Haematol. 1993 Sep;85(1):217-9.
inv(16)(p13q22)     Function of the inv(16) fusion gene CBFB-MYH11. Curr Opin Hematol. 2001 Jul;8(4):201-5.
inv(16)(p13q22)     Acute myelomonocytic leukemia associated with abnormalities of chromosome 16: a light and electron microscopic study. Hematol Pathol. 1987;1(2):105-12.
inv(16)(p13q22)     An increase in basophils in a case of acute myelomonocytic leukaemia associated with marrow eosinophilia and inversion of chromosome 16. Eur J Haematol. 1987 Nov;39(5):457-61.
inv(16)(p13q22)     Quantitative acute leukemia cytogenetics. Genes Chromosomes Cancer. 1992 Jul;5(1):57-66.
inv(16)(p13q22)     Early secondary acute myelogenous leukemia in breast cancer patients after treatment with mitoxantrone, cyclophosphamide, fluorouracil and radiation therapy. Ann Oncol. 2000 Oct;11(10):1289-94.
inv(16)(p13q22)     Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered. Oncogene. 1999 Jan 14;18(2):543-50.
inv(16)(p13q22)     Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association. N Engl J Med. 1983 Sep 15;309(11):630-6.
inv(16)(p13q22)     [Long term follow-up of three cases of acute myeloid leukemia associated with inv(16)(p13q22)] Rinsho Ketsueki. 1993 Aug;34(8):942-5.
inv(16)(p13q22)     Characterization and use of an antibody detecting the CBFbeta-SMMHC fusion protein in inv(16)/t(16;16)-associated acute myeloid leukemias. Blood. 1998 Mar 15;91(6):1882-90.
inv(16)(p13q22)     Core binding factor (CBF) acute myeloid leukemia: is molecular monitoring by RT-PCR useful clinically? Eur J Haematol. 2003 Sep;71(3):143-54.
inv(16)(p13q22)     Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001. Br J Haematol. 2003 May;121(4):566-77.
inv(16)(p13q22)     [The interest of standard and molecular cytogenetics for diagnosis of acute leukemia] Pathol Biol (Paris). 2003 Aug;51(6):337-45.
inv(16)(p13q22)     A chromosomal alteration of inv(16)(p13q22) as an additional change to t(9;11)(p22;q23) in a patient with acute monoblastic leukemia (M5a) Int J Hematol. 1998 Jan;67(1):95-7.
inv(16)(p13q22)     Chromosomal abnormalities in childhood acute nonlymphocytic leukemia (M4). Cancer Genet Cytogenet. 1991 Dec;57(2):195-200.
inv(16)(p13q22)     Core-binding factor (CBF) and MLL-associated primary acute myeloid leukemia: biology and clinical implications. Ann Hematol. 1999 Jun;78(6):251-64.
inv(16)(p13q22)     Inversion (16)(p13q22) in tumor cells of sigmoid colon. Cancer Genet Cytogenet. 1987 Jul;27(1):171-5.
inv(16)(p13q22)     Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias. Blood. 1995 Mar 1;85(5):1313-22.
inv(16)(p13q22)     Do leukemia patients with chromosome 16 inversion--inv(16)(p13q22)--have a rare fragile site at 16q22? Cancer Genet Cytogenet. 1988 Mar;31(1):31-4.
inv(16)(p13q22)     p190(BCR-ABL) rearrangement as a secondary change in a case of acute myelo-monocytic leukemia with inv(16)(p13q22). Leuk Res. 2004 Jan;28(1):97-9.
inv(16)(p13q22)     Fragile sites: overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expression. Cancer Genet Cytogenet. 1986 Jan 1;19(1-2):141-50.
inv(16)(p13q22)     Heterogeneity in CBF beta/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia. Blood. 1995 Jun 15;85(12):3695-703.
inv(16)(p13q22)     Detection of CBFB/MYH11 transcripts in patients with inversion and other abnormalities of chromosome 16 at presentation and remission. Br J Haematol. 1995 Sep;91(1):104-8.
inv(16)(p13q22)     The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: a 12-year study (1970-1982). Cancer Genet Cytogenet. 1983 Nov;10(3):219-36.
inv(16)(p13q22)     Cytogenetic studies in de novo acute nonlymphocytic leukemia. Zhonghua Yi Xue Za Zhi (Taipei). 1995 Apr;55(4):296-301.
inv(16)(p13q22)     Inversion of chromosome 16 and eosinophilia in refractory anemia with ring sideroblasts: report of a case. Am J Hematol. 1993 Oct;44(2):134-8.
inv(16)(p13q22)     Metallothionein gene cluster is split by chromosome 16 rearrangements in myelomonocytic leukaemia. Nature. 1985 Feb 21-27;313(6004):709-11.
inv(16)(p13q22)     Comment in: Clin Cancer Res. 2003 Apr;9(4):1248-52. Clin Cancer Res. 2003 Apr;9(4):1333-7.
inv(16)(p13q22)     Comment in: Cancer Genet Cytogenet. 1998 Feb;101(1):81. Cancer Genet Cytogenet. 1997 Apr;94(2):99-102.
inv(16)(p13q22)     Multicolor karyotyping in acute myeloid leukemia. Leuk Lymphoma. 2003 Nov;44(11):1843-53.
inv(16)(p13q22)     Chromosome aberrations in de novo acute myeloid leukemia patients in Kuwait. Neoplasma. 2004;51(3):223-7.
inv(16)(p13q22)     Detection of fusion transcripts generated by the inversion 16 chromosome in acute myelogenous leukemia. Blood. 1994 Apr 1;83(7):1750-6.
inv(16)(p13q22)     Molecular and clinical advances in core binding factor primary acute myeloid leukemia: a paradigm for translational research in malignant hematology. Cancer Invest. 2000;18(8):768-80.
inv(16)(p13q22)     Acute myelomonocytic leukemia with abnormal eosinophils and inv(16) or t(16;16) has a favorable prognosis. Blood. 1986 Dec;68(6):1242-9.

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