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 *

129 related articles for article (PubMed ID: 11280950)

  • 1. Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel.
    Tuck-Muller CM; Goodman BK; Li S; Martinez JE; Chen XN; Wertelecki W; Korenberg JR; Stetten G
    Genet Med; 2001; 3(2):126-31. PubMed ID: 11280950
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
    Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2q.
    Del Rey J; Santos M; González-Meneses A; Milà M; Fuster C
    Cytogenet Genome Res; 2016; 148(2-3):156-64. PubMed ID: 27216161
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503).
    Stratakis CA; Lafferty A; Taymans SE; Gafni RI; Meck JM; Blancato J
    J Clin Endocrinol Metab; 2000 Sep; 85(9):3396-401. PubMed ID: 10999840
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].
    Grasshoff U; Singer S; Liehr T; Starke H; Fode B; Schöning M; Dufke A
    Cytogenet Genome Res; 2003; 103(1-2):17-23. PubMed ID: 15004458
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A report of pure 7p duplication syndrome and review of the literature.
    Papadopoulou E; Sifakis S; Sarri C; Gyftodimou J; Liehr T; Mrasek K; Kalmanti M; Petersen MB
    Am J Med Genet A; 2006 Dec; 140(24):2802-6. PubMed ID: 17103460
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B; Kotzot D; Brecevic L; Koehler M; Balmer D; Binkert F; Schinzel A
    Eur J Hum Genet; 1999 Dec; 7(8):873-83. PubMed ID: 10602362
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA; Pai GS; Stetten G
    Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques.
    Pan Q; Hu H; Han L; Jing X; Liu H; Yang C; Zhang F; Hu Y; Yue H; Ning Y
    PLoS One; 2016; 11(5):e0154574. PubMed ID: 27218255
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients.
    Szabó GP; Knegt AC; Ujfalusi A; Balogh E; Szabó T; Oláh É
    Am J Med Genet A; 2012 Apr; 158A(4):869-76. PubMed ID: 22407767
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
    Benussi DG; Costa P; Zollino M; Murdolo M; Petix V; Carrozzi M; Pecile V
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):199-204. PubMed ID: 19378504
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridization.
    Kibbelaar RE; Mulder JW; Dreef EJ; van Kamp H; Fibbe WE; Wessels JW; Beverstock GC; Haak HL; Kluin PM
    Blood; 1993 Aug; 82(3):904-13. PubMed ID: 8338953
    [TBL] [Abstract][Full Text] [Related]  

  • 13. YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome.
    Nadal M; Milà M; Pritchard M; Mur A; Pujals J; Blouin JL; Antonarakis SE; Ballesta F; Estivill X
    Hum Genet; 1996 Oct; 98(4):460-6. PubMed ID: 8792823
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
    Petković I; Barisić I; Bastić M; Hećimović S; Bago R
    Am J Med Genet A; 2003 Jul; 120A(2):266-71. PubMed ID: 12833412
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements.
    Kaiser-Rogers KA; Rao KW; Michaelis RC; Lese CM; Powell CM
    Am J Med Genet; 2000 Nov; 95(1):28-35. PubMed ID: 11074491
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations].
    Vorsanova SG; Iurov IuB; Solov'ev IV; Demidova IA; Sharonin VO; Male R; Zhiollant M; Beresheva AK; Kolotiĭ AD; Kravets VS; Ruazes Zh
    Klin Lab Diagn; 2000 Aug; (8):36-9. PubMed ID: 11031431
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.
    Popp S; Jauch A; Schindler D; Speicher MR; Lengauer C; Donis-Keller H; Riethman HC; Cremer T
    Hum Genet; 1993 Dec; 92(6):527-32. PubMed ID: 8262510
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Severe psychomotor retardation in a boy with a supernumerary derivative chromosome resulting in partial trisomy 21 and partial trisomy 7p.
    Ahlbom BE; Wahlström J; Saalman R; Wadelius C; Annerén G
    Ann Genet; 2003; 46(1):29-35. PubMed ID: 12818527
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assessments of clonal composition of colorectal adenomas by FISH analysis of chromosomes 1, 7, 13 and 20.
    Bomme L; Lothe RA; Bardi G; Fenger C; Kronborg O; Heim S
    Int J Cancer; 2001 Jun; 92(6):816-23. PubMed ID: 11351301
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.