BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 16412230)

  • 1. Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature.
    Brooks BP; Meck JM; Haddad BR; Bendavid C; Blain D; Toretsky JA
    BMC Med Genet; 2006 Jan; 7():2. PubMed ID: 16412230
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
    Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
    Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
    Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
    Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
    Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
    Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
    Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.
    Tan EC; Lim E; Cham B; Knight L; Ng I
    Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
    Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter.
    Yamada K; Uchiyama A; Arai M; Kubodera K; Yamamoto Y; Orii KO; Nagasawa H; Masuno M; Kohno Y
    Congenit Anom (Kyoto); 2009 Jun; 49(2):85-8. PubMed ID: 19489960
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB; Lin SP; Chen CP; Chen YJ; Lee CC
    Genet Couns; 2006; 17(4):435-40. PubMed ID: 17375530
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation.
    Işik U; Başaran S; Dehgan T; Apak M
    Pediatr Neurol; 2008 Jul; 39(1):55-7. PubMed ID: 18555175
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
    Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities.
    Cox DM; Butler MG
    Cytogenet Genome Res; 2015; 145(1):29-34. PubMed ID: 25871641
    [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. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
    Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M; Wethling H; Niemeyer ML; Schwinger E
    Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.