BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

847 related articles for article (PubMed ID: 17172463)

  • 1. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
    Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
    J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Telomere capture as a frequent mechanism for stabilization of the terminal chromosomal deletion associated with inverted duplication.
    Yu S; Graf WD
    Cytogenet Genome Res; 2010; 129(4):265-74. PubMed ID: 20606397
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p.
    Schlade-Bartusiak K; Tucker T; Safavi H; Livingston J; van Allen MI; Eydoux P; Armstrong L
    Eur J Med Genet; 2013 May; 56(5):229-35. PubMed ID: 23416622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.
    Pedurupillay CR; Misceo D; Gamage TH; Dissanayake VH; Frengen E
    Gene; 2014 Jan; 533(1):403-10. PubMed ID: 24095780
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo inverted duplication 9p21pter involving telomeric repeated sequences.
    Sanlaville D; Baumann C; Lapierre JM; Romana S; Collot N; Cacheux V; Turleau C; Tachdjian G
    Am J Med Genet; 1999 Mar; 83(2):125-31. PubMed ID: 10190483
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
    Kulikowski LD; Christ LA; Nogueira SI; Brunoni D; Schwartz S; Melaragno MI
    Am J Med Genet A; 2006 Jan; 140(1):82-7. PubMed ID: 16333825
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
    Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
    Bergman A; Blennow E
    Eur J Hum Genet; 2000 Oct; 8(10):801-4. PubMed ID: 11039583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
    Rossi E; Riegel M; Messa J; Gimelli S; Maraschio P; Ciccone R; Stroppi M; Riva P; Perrotta CS; Mattina T; Memo L; Baumer A; Kucinskas V; Castellan C; Schinzel A; Zuffardi O
    J Med Genet; 2008 Mar; 45(3):147-54. PubMed ID: 18006671
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Stabilization of a terminal inversion duplication of 8p by telomere capture from 18q.
    Kostiner DR; Nguyen H; Cox VA; Cotter PD
    Cytogenet Genome Res; 2002; 98(1):9-12. PubMed ID: 12584435
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancer.
    Vukovic B; Beheshti B; Park P; Lim G; Bayani J; Zielenska M; Squire JA
    Cytogenet Genome Res; 2007; 116(1-2):1-11. PubMed ID: 17268171
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].
    Wu D; Wang H; Zhang H; Hou Q; Qin L; Wang T; Xiao H; Liao S; Wang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):823-6. PubMed ID: 26663057
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unusual 8p inverted duplication deletion with telomere capture from 8q.
    Buysse K; Antonacci F; Callewaert B; Loeys B; Fränkel U; Siu V; Mortier G; Speleman F; Menten B
    Eur J Med Genet; 2009; 52(1):31-6. PubMed ID: 19041960
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome healing of constitutional chromosome deletions studied by microdissection.
    Vermeesch JR; Falzetti D; Van Buggenhout G; Fryns JP; Marynen P
    Cytogenet Cell Genet; 1998; 81(1):68-72. PubMed ID: 9691179
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 43.