BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 16092120)

  • 1. Trisomy 20q13 --> 20qter in a girl with multiple congenital malformations and a recombinant chromosome 20 inherited from a paternal inversion (20)(p13q13.1): clinical report and review of the trisomy 20q phenotype.
    Grange DK; Garcia-Heras J; Kilani RA; Lamp S
    Am J Med Genet A; 2005 Sep; 137A(3):308-12. PubMed ID: 16092120
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: patient report and review of 20qter duplications.
    Starr LJ; Truemper EJ; Pickering DL; Sanger WG; Olney AH
    Am J Med Genet A; 2014 Aug; 164A(8):2020-4. PubMed ID: 24954807
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identical cryptic partial monosomy 20pter and trisomy 20qter in three adult siblings due to a large maternal pericentric inversion: detection by MLPA and breakpoint mapping by SNP array analysis.
    Stevens SJ; Smeets EE; Blom E; van Uum CM; Albrechts JC; Herbergs J; Janssen JW; Engelen JJ
    Am J Med Genet A; 2009 Oct; 149A(10):2226-30. PubMed ID: 19725130
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature review.
    Blanc P; Gouas L; Francannet C; Giollant M; Vago P; Goumy C
    Am J Med Genet A; 2008 May; 146A(10):1307-11. PubMed ID: 18384146
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
    Plotner PL; Smith JL; Northrup H
    Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
    Garcia-Heras J; Martin J
    Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of partial trisomy 20p resulting from meiotic recombination of a maternal pericentric inversion.
    Kang JE; Park MY; Cheon CK; Lee HD; Hwang SH; Yi J
    Ann Lab Med; 2012 Jan; 32(1):91-4. PubMed ID: 22259786
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
    Dufke A; Eggermann K; Balg S; Stengel-Rutkowski S; Enders H; Kaiser P
    Cytogenet Cell Genet; 2000; 91(1-4):85-9. PubMed ID: 11173836
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3).
    Cervera M; Sánchez S; Molina B; Alcántara MA; Del Castillo V; Carnevale A; González-del Angel A
    Am J Med Genet A; 2005 Aug; 136A(4):381-5. PubMed ID: 16001443
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.
    Leclercq S; Maincent K; Baverel F; Tessier DL; Letourneur F; Lebbar A; Dupont JM
    Am J Med Genet A; 2009 Mar; 149A(3):437-45. PubMed ID: 19206177
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion.
    Sgardioli IC; Simioni M; Viguetti-Campos NL; Prota JR; Gil-da-Silva-Lopes VL
    Gene; 2013 Jul; 523(2):192-4. PubMed ID: 23566844
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres.
    Worsham MJ; Miller DA; Devries JM; Mitchell AR; Babu VR; Surli V; Weiss L; Van Dyke DL
    Am J Hum Genet; 1989 Jan; 44(1):115-23. PubMed ID: 2909165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
    Hou JW
    Chang Gung Med J; 2005 Sep; 28(9):657-61. PubMed ID: 16323558
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).
    Delicado A; Escribano E; Lopez Pajares I; Diaz de Bustamante A; Carrasco S
    J Med Genet; 1991 Feb; 28(2):126-7. PubMed ID: 2002483
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.
    Liang D; Wu L; Pan Q; Harada N; Long Z; Xia K; Yoshiura K; Dai H; Niikawa N; Cai F; Xia J
    Am J Med Genet A; 2006 Feb; 140(3):238-44. PubMed ID: 16411213
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).
    Lansky-Shafer SC; Daniel WL; Ruiz L
    J Med Genet; 1981 Feb; 18(1):59-61. PubMed ID: 7253000
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome.
    Ounap K; Ilus T; Bartsch O
    Am J Med Genet A; 2005 May; 134(4):434-8. PubMed ID: 15793836
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.