Cytogenetics Database CytoD 1.0
Search Results:
Query: der(5)(?) Search Results: 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.
|