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Cytogenetics Database CytoD 1.0

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Query: der(7)(q?)

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der(7)t(     Clonal preservation of human pancreatic cell line derived from primary pancreatic adenocarcinoma. Pancreas. 1999 Nov;19(4):353-61.
der(7)t(     Phenotypic and genotypic diversity of human neuroblastoma studied in three IGR cell line models derived from bone marrow metastases. Cancer Genet Cytogenet. 1999 Jul 15;112(2):124-9.
der(7)t(     Novel translocation in acute megakaryoblastic leukemia (AML-M7). J Pediatr Hematol Oncol. 2003 May;25(5):396-402.
der(7)in     Cytogenetic study of malignant triton tumor: a case report. Cancer Genet Cytogenet. 2003 Jul 15;144(2):100-5.
der(7),t     Ocular anomalies in an unbalanced translocation between chromosomes 7 and 8. Bull Soc Belge Ophtalmol. 1994;254:147-55.
der(7)t(     Cytogenetic and FISH analysis of endometrial carcinoma. Cancer Genet Cytogenet. 1994 Apr;73(2):142-6.
der(7) t     Involvement of the region 13q14 in a patient with adamantinoma of the long bones. Hum Genet. 1990 Oct;85(5):513-5.
der(7)t(     Cytologic characterization of two distinct alpha satellite DNA domains on human chromosome 7, using double-labeling hybridizations in fluorescence and electron microscopy on a melanoma cell line. Cancer Genet Cytogenet. 1997 Jul 1;96(1):17-22.
der(7)t(     Trisomy 4q syndrome: presentation of a new case and review of the literature. Ann Genet. 2002 Apr-Jun;45(2):53-7.
der(7),t     46,XX,-7,+der(7),t(7;18) (q34;q21.3)mat. The pregnancy was terminated at week
der(7)t(     A hamartoma of the breast with an aberration of 12q mapped to the MAR region by fluorescence in situ hybridization. Cancer Genet Cytogenet. 1995 Oct 1;84(1):82-4.
der(7)t(     Reproductive risk in mating between two translocation carriers: case report and review of the literature. Am J Med Genet. 1993 Jun 15;46(5):524-8.
der(7)t(     Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma. Br J Haematol. 2001 Jan;112(1):167-74.
der(7)t(     Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia. Genes Chromosomes Cancer. 2003 Oct;38(2):191-200.
der(7)t(     Chromosome analysis of a newly established renal carcinoma cell line. Cancer Genet Cytogenet. 1988 Jul 1;33(1):133-8.
der(7)t(     Chromosome analysis of parallel short-term cultures from four testicular germ-cell tumors. Cancer Genet Cytogenet. 1994 Jul 15;75(2):90-102.
der(7)t(     Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma. Cancer Genet Cytogenet. 1989 Jun;39(2):227-32.
der17t(7     Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1). Am J Med Genet. 1989 Nov;34(3):358-65.
der(7)t(     Molecular characterization of trisomic segment 3p24.1-->3pter: a case with review of the literature. Clin Genet. 1995 Jul;48(1):49-53.
der(7)(5     A complex translocation (5;7) in a patient with acute nonlymphocytic leukemia evolved from a myelodysplastic syndrome. Cancer Genet Cytogenet. 1998 Sep;105(2):182-6.
der(7)t(     Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis. Am J Med Genet. 1993 Jun 15;46(5):559-62.
der(7),d     Biclonal chromosome evolution of chronic myelomonocytic leukemia in a child. Cancer Genet Cytogenet. 1990 Jan;44(1):131-7.
der(7)t(     A third case of a low-grade endometrial stromal sarcoma with a t(7;17)(p14 approximately 21;q11.2 approximately 21). Cancer Genet Cytogenet. 1997 Oct 1;98(1):84-6.
der(7)(7     Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene? Hum Genet. 1995 Oct;96(4):485-9.
der(7)t(     Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly. Clin Genet. 1996 Nov;50(5):321-6.
der(7)t(     Recessive cancer genes in meningiomas? An analysis of 31 cases. Cancer Genet Cytogenet. 1987 Jul;27(1):145-59.
der(7) t     Agranular CD4+CD56+ blastic natural killer leukemia/lymphoma. Ann Hematol. 2001 Apr;80(4):228-31.
der(7)t(     Cytogenetic characterization of the human prostate cancer cell line P69SV40T and its novel tumorigenic sublines M2182 and M15. Cancer Genet Cytogenet. 1996 Mar;87(1):14-23.
der(7)t(     A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q. J Med Genet. 1997 Sep;34(9):772-6.
der17) d     Derivative chromosome 17 in a case of Burkitt lymphoma with 8;14 translocation. Cancer Genet Cytogenet. 1999 Apr;110(1):1-6.
der(7),t     [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)] Ann Genet. 1984;27(4):241-4.
der(7)t(     Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotype. Ann Genet. 1990;33(2):111-2.
der(7)t(     Analysis by pulsed field gel electrophoresis reveals complex rearrangements in two MET alleles in a chemically-treated human cell line, MNNG-HOS. Oncogene. 1990 Oct;5(10):1565-71.
der(7),      Cytogenetic investigation of canine lipomas. Cancer Genet Cytogenet. 1999 Jun;111(2):172-4.
der(7) d     Partial triplication (7q) in a child with acute lymphoblastic leukemia demonstrated with conventional cytogenetics, PRINS, and chromosome painting. Cancer Genet Cytogenet. 1995 Oct 1;84(1):19-23.
der(7;12     Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies. Genes Chromosomes Cancer. 1995 Sep;14(1):56-62.
der(7)t(     Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients. Blood. 1989 Oct;74(5):1781-90.
der(7) t     Chromosome abnormalities in a pancreatic adenocarcinoma. Cancer Genet Cytogenet. 1989 Feb;37(2):209-13.
der(7)t(     Cytogenetic analysis of two sacral chordomas. Cancer Genet Cytogenet. 1991 Oct 15;56(2):197-201.
der(7)(n     Deletion 6p23 and add(11)(p15) leading to NUP98 translocation in a case of therapy-related atypical chronic myelocytic leukemia transforming to acute myelocytic leukemia. Cancer Genet Cytogenet. 2004 Jul 1;152(1):56-60.
der(7) d     Molecular cloning of a constitutional t(7;22) translocation associated with risk of hematological malignancy. Genes Chromosomes Cancer. 2003 Nov;38(3):260-4.
der(7)t(     Translocation t(12;22)(q13;q12.2-12.3) in a clear cell sarcoma of tendons and aponeuroses. Genes Chromosomes Cancer. 1993 Apr;6(4):249-52.
der(7) t     Uncommon cytogenetic findings in a case of splenic marginal zone lymphoma with aggressive clinical course. Cancer Genet Cytogenet. 2004 Jan 15;148(2):133-6.
der(7)t(     Cytogenetic findings in a pleomorphic xanthoastrocytoma. Cancer Genet Cytogenet. 1991 Sep;55(2):225-30.
der(7)t(     Clonal involvement of eosinophils in therapy-related myelodysplastic syndrome with eosinophilia, translocation t(1;7) and lung cancer. Br J Haematol. 1996 Dec;95(4):710-4.
der(7)t(     Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia. Prenat Diagn. 1999 Oct;19(10):986-9.
der(7)t(     Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia. Cancer Genet Cytogenet. 2004 Mar;149(2):125-30.
der(7)t(     A 5;7, 5;12 double reciprocal translocation in a normal mother and a 5;7 translocation with a recombinant chromosome 5 in her normal child. J Med Genet. 1981 Aug;18(4):307-9.
der(7) d     Delineation of multiple deleted regions in 7q in myeloid disorders. Genes Chromosomes Cancer. 1999 Aug;25(4):384-92.
der(7) t     Establishment of a human pancreatic tumor xenograft model: potential application for preclinical evaluation of novel therapeutic agents. Pancreas. 1998 Jan;16(1):19-25.
der(7)t(     Unbalanced translocation (1;7) and inversion 16 in a patient with acute myelocytic leukemia. Leuk Res. 1993 Aug;17(8):699-701.
der(7)t(     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.
der(7) t     Consistent breakage between consensus recombinase heptamers of chromosome 9 DNA in a recurrent chromosomal translocation of human T cell leukemia. J Exp Med. 1989 Feb 1;169(2):369-77.
der(7)t(     Significance of chromosomal abnormalities in a malignant giant cell tumor of bone. Cancer Genet Cytogenet. 1991 Nov;57(1):87-92.
der(7)de     An unusual cytogenetic abnormality involving chromosomes 1 and 7 in a case of chronic myelomonocytic leukemia. Cancer Genet Cytogenet. 1995 Nov;85(1):75-7.
der(7)t(     Cytogenetics of a case of cardiac myxoma. Cancer Genet Cytogenet. 1992 Oct 1;63(1):73-5.
der(7) d     Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3. Am J Hum Genet. 1996 Nov;59(5):999-1005.
der(7)t(     Chromosomal alterations associated with evolution from myelodysplastic syndrome to acute myeloid leukemia. Leuk Res. 2000 Oct;24(10):839-48.
der(7) d     A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome. Cancer Genet Cytogenet. 2004 Apr 1;150(1):81-5.
der(7)t(     Two rearranged MET alleles in MNNG-HOS cells reveal the orientation of MET on chromosome 7 to other markers tightly linked to the cystic fibrosis locus. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2667-71.
der(7)in     CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics. 2003 Jul;82(1):1-9.
der(7)t(     A case of adult T-cell leukaemia/lymphoma characterized by multiplex-fluorescence in situ hybridization, comparative genomic hybridization, fluorescence in situ hybridization and cytogenetics. Br J Dermatol. 2001 Jul;145(1):117-22.
der(7)t(     Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency.. Clin Genet. 2000 May;57(5):388-93.
der(7)t(     Immunophenotypic and cytogenetic analysis of Molt-3 and Molt-4: human T-lymphoid cell lines with rearrangement of chromosome 7. Blood. 1988 Nov;72(5):1755-60.
der(7)t(     Characterization of a highly aberrant plasma cell leukemia karyotype: a case report. Oncol Rep. 2004 Jan;11(1):89-92.
der(7)t(     Rearrangements involving 12p12 in two cases of cardiac myxoma. Cancer Genet Cytogenet. 1995 Jul 15;82(2):161-2.
der(7)t(     Derivative (7)t(7;8)(q34;q21). a new additional cytogenetic abnormality in acute promyelocytic leukemia. Cancer Genet Cytogenet. 2003 Jan 1;140(1):78-81.
der(7)t(     A comprehensive karyotypic analysis on a newly developed hepatocellular carcinoma cell line, HKCI-1, by spectral karyotyping and comparative genomic hybridization. Cancer Genet Cytogenet. 2000 Aug;121(1):9-16.
der(7)t(     Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH. Genes Chromosomes Cancer. 2002 Jan;33(1):60-72.
der(7) 4     A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility. Hum Reprod. 2001 Jan;16(1):59-62.
der(7)(qt     Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia. Cancer Genet Cytogenet. 2002 Apr 15;134(2):138-41.
der(7)t(     Characterization of three hairy cell leukemia- derived cell lines (ESKOL, JOK-1, and hair-M) by multiplex-FISH, comparative genomic hybridization, FISH, PRINS, and dideoxyPRINS. Cytogenet Cell Genet. 2000;90(1-2):30-9.
der(7)t(     Karyotypic analyses of hepatoblastoma. Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease. Cancer Genet Cytogenet. 1999 Oct 1;114(1):42-50.
der(7;9)     Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. The NOPHO Leukemia Cytogenetic Study Group. Eur J Haematol. 2000 Mar;64(3):194-200.
der(7)t(     A novel chromosomal rearrangement associated with therapy-related acute leukemia. Cancer Genet Cytogenet. 1999 Jul 15;112(2):173-7.
der(7)t(     Spectral karyotypic study of the HL-60 cell line: detection of complex rearrangements involving chromosomes 5, 7, and 16 and delineation of critical region of deletion on 5q31.1. Cancer Genet Cytogenet. 1999 Sep;113(2):105-9.
der(7)t(     [Study of chromosome painting for one rare carrier with complex translocation] Yi Chuan Xue Bao. 1996;23(4):255-60.
der(7),      Genomic rearrangements involving rDNA and centromeric heterochromatin in vulvar epidermoid carcinoma cell line A-431. Cancer Genet Cytogenet. 2003 May;143(1):50-8.
der(7) t     Molecular analysis of the T-cell acute lymphoblastic leukemia-associated t(1;7)(p34;q34) that fuses LCK and TCRB. Blood. 1994 Aug 15;84(4):1232-6.
der(7)t(     Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis. Leukemia. 1989 Jan;3(1):36-41.
der(7),      Chromosomal translocations joining LCK and TCRB loci in human T cell leukemia. J Exp Med. 1991 Oct 1;174(4):867-73.

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