These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

99 related articles for article (PubMed ID: 2065319)

  • 21. Embryonal rhabdomyosarcoma with 100 chromosomes but no structural aberrations.
    Olegård C; Mandahl N; Heim S; Willén H; Leifsson B; Mitelman F
    Cancer Genet Cytogenet; 1992 Jun; 60(2):198-201. PubMed ID: 1606566
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Chromosome abnormalities in a primary adult embryonal rhabdomyosarcoma of the prostate.
    Middel P; Gunawan B; Gross AJ; Radzun HJ; Füzesi L
    Histopathology; 2000 Oct; 37(4):378-80. PubMed ID: 11184186
    [No Abstract]   [Full Text] [Related]  

  • 23. Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.
    Tharapel SA; Lewandowski RC; Tharapel AT; Wilroy RS
    J Med Genet; 1986 Aug; 23(4):310-5. PubMed ID: 3746829
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms.
    Mertens F; Johansson B; Höglund M; Mitelman F
    Cancer Res; 1997 Jul; 57(13):2765-80. PubMed ID: 9205089
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma.
    Steenman M; Tomlinson G; Westerveld A; Mannens M
    Cytogenet Cell Genet; 1999; 86(2):157-61. PubMed ID: 10545709
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Trisomy 8 in primary esthesioneuroblastoma.
    VanDevanter DR; George D; McNutt MA; Vogel A; Luthardt F
    Cancer Genet Cytogenet; 1991 Nov; 57(1):133-6. PubMed ID: 1756479
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Recurrent cytogenetic aberrations in human ovarian carcinomas.
    Kiechle-Schwarz M; Bauknecht T; Schmidt J; Walz L; Pfleiderer A
    Cancer Detect Prev; 1995; 19(3):234-43. PubMed ID: 7750111
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
    Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clonal karyotype evolution in solid tumours in children.
    Orye E; Delbeke MJ
    Oncology; 1974; 29(6):520-33. PubMed ID: 4474644
    [No Abstract]   [Full Text] [Related]  

  • 34. Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities.
    Wisniewski L; Higgins JV
    J Med Genet; 1977 Oct; 14(5):378-81. PubMed ID: 592355
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A variant (2;13) translocation in rhabdomyosarcoma.
    Dal Cin P; Brock P; Aly MS; Casteels-Van Daele M; De Wever I; Van Damme B; Van den Berghe H
    Cancer Genet Cytogenet; 1991 Sep; 55(2):191-5. PubMed ID: 1933821
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cytogenetic study of a spindle-cell rhabdomyosarcoma of the parotid gland.
    Gil-Benso R; Carda-Batalla C; Navarro-Fos S; Pellín-Perez A; Llombart-Bosch A
    Cancer Genet Cytogenet; 1999 Mar; 109(2):150-3. PubMed ID: 10087951
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Frequency and pattern of karyotypic abnormalities in human prostate cancer.
    Brothman AR; Peehl DM; Patel AM; McNeal JE
    Cancer Res; 1990 Jun; 50(12):3795-803. PubMed ID: 2340524
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clonal karyotypic evolution in an embryonal rhabdomyosarcoma with trisomy 8 as the primary chromosomal abnormality.
    Dietrich CU; Jacobsen BB; Starklint H; Heim S
    Genes Chromosomes Cancer; 1993 Aug; 7(4):240-4. PubMed ID: 7692951
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.