BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 17161033)

  • 21. 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]  

  • 22. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
    Cockwell AE; Dávalos IP; Rivera HR; Crolla JA
    Am J Med Genet; 2001 Nov; 103(4):289-94. PubMed ID: 11746008
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.
    Gimelli G; Giorda R; Beri S; Gimelli S; Zuffardi O
    Eur J Med Genet; 2007; 50(4):264-73. PubMed ID: 17567547
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter.
    Knight LA; Lipson M; Mann J; Bachman R
    Am J Med Genet; 1984 Mar; 17(3):649-54. PubMed ID: 6585144
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
    Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H
    Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
    Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida.
    Gustavsson P; Schoumans J; Staaf J; Borg A; Nordenskjöld M; Annerén G
    Eur J Med Genet; 2007; 50(3):237-41. PubMed ID: 17387046
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.
    Ciuladaite Z; Preiksaitiene E; Utkus A; Kučinskas V
    Cytogenet Genome Res; 2014; 144(2):109-13. PubMed ID: 25401700
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Direct tandem duplication in chromosome 19q characterized by array CGH.
    Palomares Bralo M; Delicado A; Lapunzina P; Velázquez Fragua R; Villa O; Angeles Mori M; Luisa de Torres M; Fernández L; Pérez Jurado LA; López Pajares I
    Eur J Med Genet; 2008; 51(3):257-63. PubMed ID: 18342596
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Comparative genomic hybridization-assisted prenatal diagnosis of a de novo inverted duplication of chromosome 10q. A case report.
    Chen CK; Chang SD; Chen YJ; Hsueh DW; Soong YK
    J Reprod Med; 2003 May; 48(5):391-4. PubMed ID: 12815917
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
    Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
    Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
    Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Genetic analysis of chorionic villi specimen in spontaneous abortion using various methods].
    Lei Q; Wang Q; Zhou CQ; Chen BJ; Chen Z; Xu YW; Zeng YH
    Zhonghua Fu Chan Ke Za Zhi; 2009 Apr; 44(4):253-6. PubMed ID: 19570460
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
    Karaoguz MY; Biri A; Pala E; Kan D; Poyraz A; Kurdoglu M; Percin EF
    Genet Couns; 2006; 17(2):197-204. PubMed ID: 16970038
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis.
    Stumm M; Klopocki E; Gasiorek-Wiens A; Knoll U; Wirjadi D; Sarioglu N; Wegner RD; Tönnies H
    Prenat Diagn; 2007 May; 27(5):475-8. PubMed ID: 17330228
    [TBL] [Abstract][Full Text] [Related]  

  • 37. U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.
    Rowe LR; Lee JY; Rector L; Kaminsky EB; Brothman AR; Martin CL; South ST
    J Med Genet; 2009 Oct; 46(10):694-702. PubMed ID: 19293169
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics.
    Afifi HH; Zaki MS; El-Gerzawy AM; Kayed HF
    Genet Couns; 2008; 19(1):47-58. PubMed ID: 18564501
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q.
    Bonaglia MC; Giorda R; Poggi G; Raggi ME; Rossi E; Baroncini A; Giglio S; Borgatti R; Zuffardi O
    Eur J Hum Genet; 2000 Aug; 8(8):597-603. PubMed ID: 10951522
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.