BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 9216728)

  • 1. Involvement of 8q, 22q, and monosomy 21 in an epithelioid sarcoma.
    Sonobe H; Ohtsuki Y; Sugimoto T; Shimizu K
    Cancer Genet Cytogenet; 1997 Jul; 96(2):178-80. PubMed ID: 9216728
    [No Abstract]   [Full Text] [Related]  

  • 2. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J; Chernos J; Roland B
    Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Proximal-type epithelioid sarcoma: case report and result of comparative genomic hybridization.
    Lee MW; Jee KJ; Ro JY; Lee DP; Choi JH; Moon KC; Koh JK
    J Cutan Pathol; 2004 Jan; 31(1):67-71. PubMed ID: 14675288
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic characterization of proximal-type epithelioid sarcoma.
    Lualdi E; Modena P; Debiec-Rychter M; Pedeutour F; Teixeira MR; Facchinetti F; Dagrada GP; Pilotti S; Sozzi G
    Genes Chromosomes Cancer; 2004 Nov; 41(3):283-90. PubMed ID: 15334553
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Higher percentage of FISH-determined monosomy 3 and 8q amplification in uveal melanoma cells relate to poor patient prognosis.
    van den Bosch T; van Beek JG; Vaarwater J; Verdijk RM; Naus NC; Paridaens D; de Klein A; Kiliç E
    Invest Ophthalmol Vis Sci; 2012 May; 53(6):2668-74. PubMed ID: 22427574
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
    López-Pajares I; Martin-Ancel A; Cabello P; Delicado A; Garcia-Alix A; San Roman C
    Clin Genet; 1993 Feb; 43(2):94-7. PubMed ID: 8448910
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two subclones in a case of uveal melanoma. Relevance of monosomy 3 and multiplication of chromosome 8q.
    Prescher G; Bornfeld N; Becher R
    Cancer Genet Cytogenet; 1994 Oct; 77(2):144-6. PubMed ID: 7954325
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal hyperdiploidy in a feline sarcoma.
    Kalat M; Mayr B; Schleger W; Wagner B; Reifinger M
    Res Vet Sci; 1991 Sep; 51(2):227-8. PubMed ID: 1788488
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epithelioid sarcoma of the proximal type with complex karyotype including i(8q).
    Dal Cin P; Van den Berghe H; Pauwels P
    Cancer Genet Cytogenet; 1999 Oct; 114(1):80-2. PubMed ID: 10526542
    [No Abstract]   [Full Text] [Related]  

  • 11. Autosomal mendelian disorders and microcytogenetics.
    de Grouchy J; Turleau C
    Recenti Prog Med; 1990 May; 81(5):337-43. PubMed ID: 2198645
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Monosomy 3 and isochromosome 8q in a uveal melanoma.
    Horsman DE; Sroka H; Rootman J; White VA
    Cancer Genet Cytogenet; 1990 Apr; 45(2):249-53. PubMed ID: 2317773
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).
    Romain DR; Goldsmith J; Cairney H; Columbano-Green LM; Smythe RH; Parfitt RG
    J Med Genet; 1990 Sep; 27(9):588-9. PubMed ID: 2231653
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
    Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Combined molecular genetic studies of chromosome 22q and the neurofibromatosis type 2 gene in central nervous system tumors.
    Ng HK; Lau KM; Tse JY; Lo KW; Wong JH; Poon WS; Huang DP
    Neurosurgery; 1995 Oct; 37(4):764-73. PubMed ID: 8559307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A cell culture, chromosomal and quantitative DNA analysis of a metastatic epithelioid sarcoma. Deletion 1p, a possible primary chromosomal abnormality in epithelioid sarcoma.
    Stenman G; Kindblom LG; Willems J; Angervall L
    Cancer; 1990 May; 65(9):2006-13. PubMed ID: 2196989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. t(12;22)(q13;q13) and trisomy 8 are nonrandom aberrations in clear-cell sarcoma.
    Rodriguez E; Sreekantaiah C; Reuter VE; Motzer RJ; Chaganti RS
    Cancer Genet Cytogenet; 1992 Dec; 64(2):107-10. PubMed ID: 1486558
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Abnormally banded region in a poorly differentiated sarcoma is not correlated with amplification of c-MYC or c-MOS protooncogenes.
    Kakati S; Limon J; Dal Cin P; Pietrzak E; Kinniburgh AJ; Li FP; Sandberg AA
    Cancer Genet Cytogenet; 1988 Aug; 34(1):111-5. PubMed ID: 3395984
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial trisomy 8q and partial monosomy 18p: a case report.
    Puvabanditsin S; Garrow E; Rabi FA; Titapiwatanakun R; Kuniyoshi KM
    Ann Genet; 2004; 47(4):399-403. PubMed ID: 15581839
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epithelioid sarcoma with an 18q aberration.
    Iwasaki H; Ohjimi Y; Ishiguro M; Isayama T; Kaneko Y; Yoh S; Emoto G; Kikuchi M
    Cancer Genet Cytogenet; 1996 Oct; 91(1):46-52. PubMed ID: 8908166
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.