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Cytogenetics Database CytoD 1.0

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Query: der(5)(?)

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der(5) d     Cytogenetic study of 11 gastric adenocarcinomas. Cancer Genet Cytogenet. 1995 Jun;81(2):169-72.
der(5)t(     A chromosome study of three ovarian tumors. Cancer Genet Cytogenet. 1987 Jun;26(2):327-37.
der(5)t(     Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection. Obstet Gynecol. 1987 Sep;70(3 Pt 2):449-52.
der(5)t(     Rearrangement of the long arm of chromosome 10 in the prostate adenocarcinoma cell line LNCaP. Cancer Genet Cytogenet. 1998 Apr 1;102(1):6-11.
der(5),      Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts. Genes Chromosomes Cancer. 2004 Dec;41(4):395-9.
der(5)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(5)t(     der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder. Cancer Genet Cytogenet. 1991 Jul 1;54(1):129-31.
der(5)t(     Interstitial deletion of the short arm of chromosome 12 during clonal evolution in myelodysplastic syndrome with t(5;12)(q13;p13) involving the ETV6 gene. Cancer Genet Cytogenet. 2000 Jun;119(2):113-7.
der(5)(5     Erratum in: Genes Chromosomes Cancer. 2003 Jul;37(3):332. Genes Chromosomes Cancer. 2003 Jul;37(3):270-81.
der(5)      Nonmosaic smallest duplication of 12q24.31-qter: the first reported case. Am J Med Genet. 2004 Jul 30;128A(3):305-10.
der(5),t     The genetic events of HPV-immortalized esophageal epithelium cells. Int J Mol Med. 2001 Nov;8(5):537-42.
der(5) 4     Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier. Prenat Diagn. 2001 Mar;21(3):171-5.
der(5)t(     Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization. Blood. 1993 Jul 15;82(2):547-51.
der(5)t(     Myelodysplastic syndrome progresses rapidly into erythroleukemia associated with synchronous double cancers of the stomach and the papilla of Vater. Int J Hematol. 2001 Jul;74(1):64-9.
der(5)t(     Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma. Cancer Genet Cytogenet. 1989 Jun;39(2):227-32.
der(5)t(     Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals. Hum Genet. 2000 Jul;107(1):51-7.
der(5),      Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma. Cancer Genet Cytogenet. 1988 Feb;30(2):323-7.
der(5)t(     'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations. J Med Genet. 1977 Aug;14(4):271-4.
der(5)(5     A Y/5 translocation in a 45,X male with cri du chat syndrome. Hum Genet. 1987 Oct;77(2):145-50.
der(5)in     A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: a case report. Cancer Genet Cytogenet. 1993 Feb;65(2):141-6.
der(5)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(5),      Unusual distribution of chromosome 12 in a testicular germ-cell tumor cell line (833K) and its cisplatin-resistant derivative (64CP9). Cancer Genet Cytogenet. 1993 Jul 15;68(2):114-21.
der(5)t(     Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9. Am J Med Genet. 1993 Jan 1;45(1):77-80.
der(5)t(     Translocation (5;22) in an Askin's tumor. Cancer Genet Cytogenet. 1992 Sep;62(2):203-5.
der(5)(5     Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome. Am J Med Genet. 2001 Dec 15;104(4):312-8.
der(5)t(     Non-reciprocal translocation (5;15), isodicentric (15) and Prader-Willi syndrome. Am J Med Genet. 1986 Sep;25(1):61-9.
der(5)t(     Discrepant cytogenetic and fluorescence in situ hybridization results in a 26-year-old male with early T-cell acute lymphocytic leukemia. Cancer Genet Cytogenet. 1998 Oct 15;106(2):116-21.
der(5)t(     Clinical features and mental development of a child with a prenatally identified 45,XX,der(5)t(5;18) (p15;q11.2),-18 karyotype. J Med Genet. 1998 Oct;35(10):865-7.
der(5)t(     Atypical response to all-trans retinoic acid in a der(5)t(5;17) acute promyelocytic leukemia. Leukemia. 1999 Jun;13(6):862-8.
der(5)(5     Characterization of a new EBV-associated nasopharyngeal carcinoma cell line. Cancer Genet Cytogenet. 1998 Mar;101(2):83-8.
der(5)t(     Unbalanced translocation t(5;17) in an typical acute promyelocytic leukemia. Genes Chromosomes Cancer. 1995 Dec;14(4):307-12.
der(5)t(     Complex karyotypic anomalies in a bizarre leiomyoma of the uterus. Genes Chromosomes Cancer. 1989 Nov;1(2):131-4.
der(5),t     Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;;14) (pter;q11.2)]. Am J Med Genet. 2001 Jul 22;102(1):29-35.
der(5),t     Partial distal trisomy 13q resulting from familial reciprocal 5/13 translocation. Hum Genet. 1978 Dec 29;45(3):345-50.
der(5)t(     Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization. Clin Genet. 2004 Jun;65(6):477-82.
der(5),t     Cri-Du-Chat syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat Karyotype. Hum Genet. 1977 Nov 2;39(1):109-12.
der(5)(:     Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities. Prenat Diagn. 1996 Oct;16(10):915-22.
der(5) t     Translocation (3;5)(q21;q34) in erythroleukemia: a molecular and in situ hybridization study. Cancer Genet Cytogenet. 1998 May;103(1):15-9.
der(5;17     Deletions of chromosome 5q13.3 and 17p loci cooperate in myeloid neoplasms. Blood. 2000 Mar 15;95(6):2138-43.
der(5)t(     Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome. J Med Genet. 1997 Oct;34(10):819-26.
der(5),t     Simultaneous trisomy 9q3 and monosomy 5p in two children with der(5),t(5;9)(p15.1;q34.13): report of an extended family. J Med Genet. 1988 Oct;25(10):707-10.
der(5)t(     Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature. Cancer Genet Cytogenet. 1992 Jan;58(1):66-70.
der(5)t(     Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization. Cancer Genet Cytogenet. 2000 Apr 1;118(1):1-8.
der(5) t     Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study. Hum Genet. 1990 Aug;85(3):337-42.
der(5)t(     A case of acute nonlymphocytic leukemia with a derivative chromosome 5 resulting from a subtle unbalanced translocation, der(5)t(5;17)(p15.3;q25.1). Cancer Genet Cytogenet. 1997 Aug;97(1):73-5.
der(5)t(     Erratum in: Genomics 1992 Nov;14(3):832. Genomics. 1991 Nov;11(3):701-8.
der(5) t     Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation. J Med Genet. 1977 Feb;14(1):68-72.
der(5)t(     Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party. Groupe Français de Cytogénétique Hématologique, Groupe de Français d'Hematologie Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concerted Action "Molecular Cytogenetic Diagnosis in Haematological Malignancies". Blood. 2000 Aug 15;96(4):1297-308.
der(5),t     Cytogenetic changes at 11q11, 11q23, and 17q11 in myelodysplastic syndrome. Cancer Genet Cytogenet. 1986 Apr 15;21(4):287-95.
der(5) t     Detection of the t(2;5)(p23;q35) and NPM-ALK fusion in non-Hodgkin's lymphoma by two-color fluorescence in situ hybridization. Blood. 1997 Mar 1;89(5):1678-85.
der(5;15     Cytogenetic abnormalities in a squamous cell carcinoma of the penis. Cancer Genet Cytogenet. 1992 Dec;64(2):139-41.
der(5)t(     Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinoma. Cancer. 1990 Sep 15;66(6):1213-20.
der(5)t(     Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. Cancer Res. 1999 Jan 1;59(1):141-50.
der(5)t(     Acute erythroleukemia with t(3;5) accompanied by hepatocellular carcinoma. Int J Hematol. 1991 Jun;54(3):213-7.
der(5)t(     Tumor behavior in transitional cell carcinoma of the bladder in relation to chromosomal markers and histopathology. Cancer Res. 1987 Dec 15;47(24 Pt 1):6800-5.
der(5)t(     :20p11.1-->20p13),del(2)(q12),der(3)t(3;6),der(5)t(5;18)
der(5)      Cellular and genetic constitution of human endometriosis tissues. J Soc Gynecol Investig. 2000 Mar-Apr;7(2):79-87.
der(5)t(     Double minutes arise from circular extrachromosomal DNA intermediates which integrate into chromosomal sites in human HL-60 leukemia cells. J Clin Invest. 1990 Jun;85(6):1887-95.
der(5),      Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect. Genet Couns. 1990;1(2):179-84.
der(5)t(     Stromal cells and human malignant neuroblasts derived from bone marrow metastasis may share common karyotypic abnormalities: the case of the IGR-N-91 cell line. Med Pediatr Oncol. 2001 Jan;36(1):100-3.
der(5)t(     Characterization of a highly aberrant plasma cell leukemia karyotype: a case report. Oncol Rep. 2004 Jan;11(1):89-92.
der(5)t(     dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53. Genes Chromosomes Cancer. 1997 Nov;20(3):282-91.
der(5)t(     Comprehensive molecular cytogenetic characterization of cervical cancer cell lines. Genes Chromosomes Cancer. 2003 Mar;36(3):233-41.
der(5)t(     A synovial sarcoma with a complex t(X;18;5;4) and a break in the ornithine aminotransferase (OAT)L1 cluster on Xp11.2. Genes Chromosomes Cancer. 1994 Apr;9(4):288-91.
der(5) d     Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy. Am J Hum Genet. 1995 Aug;57(2):329-36.
der15,t(     Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization. Am J Med Genet. 1994 Mar 1;50(1):21-7.
der(5)t(     Translocation (1;5)(q23;q33) in adult acute non-lymphocytic leukemia. Eur J Haematol. 1989 Mar;42(3):246-9.
der(5)t(     Der(5)t(5;7)(q11.2;p11.2): a new recurring abnormality in malignant myeloid disorders. Cancer Genet Cytogenet. 1989 Jan;37(1):1-8.
der(5)t(     Near-haploidy in a malignant sacrococcygeal teratoma. Cancer Genet Cytogenet. 1999 Jan 1;108(1):70-4.
der(5)t(     Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. Am J Med Genet. 1993 Sep 1;47(3):387-91.
der(5)t(     Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques. Prenat Diagn. 2003 Sep;23(9):747-51.
der(5)/d     TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13). Blood. 1995 May 15;85(10):2848-52.
der(5)t(     Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization. Cytogenet Cell Genet. 1997;76(1-2):68-71.
der(5)t(     Acute promyelocytic leukemia with additional chromosomal abnormalities and absence of Auer rods. Am J Clin Pathol. 1999 Jul;112(1):113-8.
der(5) t     Genetic abnormalities detected by comparative genomic hybridization in a human endometriosis-derived cell line. Mol Hum Reprod. 2000 Sep;6(9):821-7.
der(5)t(     Overexpression of the BCL2 gene in a Sertoli-Leydig cell tumor of the ovary: a pathologic and cytogenetic study. Cancer Genet Cytogenet. 2004 Jan 15;148(2):118-22.


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