BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

561 related articles for article (PubMed ID: 15004458)

  • 1. 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]  

  • 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. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.
    Cai T; Yu P; Tagle DA; Lu D; Chen Y; Xia J
    Hum Reprod; 2001 Jan; 16(1):59-62. PubMed ID: 11139537
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
    Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.
    Wu D; Zhang H; Hou Q; Wang H; Wang T; Liao S
    Mol Med Rep; 2017 Nov; 16(5):6222-6227. PubMed ID: 28901405
    [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. Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation.
    Fan J; Senaratne TN; Liu JY; Bina M; Martinez-Agosto JA; Quintero-Rivera F; Wang JJ
    BMC Med Genomics; 2023 Mar; 16(1):65. PubMed ID: 36991446
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of a balanced complex chromosomal rearrangement carrier ascertained through a fetus with dup15q26.3 and del5p15.33: case report.
    Lledo B; Ortiz JA; Morales R; Manchon I; Galan F; Bernabeu A; Bernabeu R
    Hum Fertil (Camb); 2013 Sep; 16(3):215-7. PubMed ID: 23905868
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
    Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
    Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
    Dufke A; Mayrhofer H; Enders H; Kaiser P; Leipoldt M
    Cytogenet Cell Genet; 2001; 93(3-4):168-70. PubMed ID: 11528107
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).
    Plomp AS; Engelen JJ; Albrechts JC; de Die-Smulders CE; Hamers AJ
    J Med Genet; 1998 Jul; 35(7):604-8. PubMed ID: 9678708
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation.
    Sun SC; Luo FW; Song HW; He JB; Peng YS
    J Int Med Res; 2009; 37(4):1230-7. PubMed ID: 19761709
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Complex chromosome rearrangement involving chromosomes 1, 4 and 16 revealed by fluorescence in situ hybridization.
    Johannesson T; Ehlers S; Wahlström J
    Clin Genet; 1997 Apr; 51(4):281-5. PubMed ID: 9184255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 29.