BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 15845171)

  • 1. Duplication of the 22q11.2 region associated with congenital cardiac disease.
    Sparkes R; Chernos J; Dicke F
    Cardiol Young; 2005 Apr; 15(2):229-31. PubMed ID: 15845171
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Concurrent microdeletion and duplication of 22q11.2.
    Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
    Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation dependent probe amplification].
    Yang YH; Hu YL; Zhu XY; Mo XM; Wang DJ; Yao JC; Sheng M; Zhu HY; Li J; Ru T; Wang ZQ
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Nov; 11(11):892-6. PubMed ID: 20113655
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
    Hu Y; Zhu X; Yang Y; Mo X; Sheng M; Yao J; Wang D
    Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G; Alvares S; Rocha C; Teixeira MF; Mota MC; Reis MI; Feijó MJ; Lima MR; Pinto MR
    Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital cardiopathies and syndromes in adults].
    Calderón Colmenero J
    Arch Cardiol Mex; 2002; 72 Suppl 1():S31-4. PubMed ID: 12001867
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication of (12)(pter-q13.3) combined with deletion of (22)(pter-q11.2) in a patient with features of both chromosome aberrations.
    Tyshchenko NA; Riegel M; Evseenkova EG; Zerova TE; Gorovenko NG; Schinzel A
    Eur J Med Genet; 2007; 50(2):128-32. PubMed ID: 17174617
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
    Stalmans I
    Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
    Coppinger J; McDonald-McGinn D; Zackai E; Shane K; Atkin JF; Asamoah A; Leland R; Weaver DD; Lansky-Shafer S; Schmidt K; Feldman H; Cohen W; Phalin J; Powell B; Ballif BC; Theisen A; Geiger E; Haldeman-Englert C; Shaikh TH; Saitta S; Bejjani BA; Shaffer LG
    Hum Mol Genet; 2009 Apr; 18(8):1377-83. PubMed ID: 19193630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases.
    Gioli-Pereira L; Pereira AC; Bergara D; Mesquita S; Lopes AA; Krieger JE
    Int J Cardiol; 2008 Jun; 126(3):374-8. PubMed ID: 17604138
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microduplication 22q11.2: a new chromosomal syndrome.
    Portnoï MF
    Eur J Med Genet; 2009; 52(2-3):88-93. PubMed ID: 19254783
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autistic disorder and 22q11.2 duplication.
    Mukaddes NM; Herguner S
    World J Biol Psychiatry; 2007; 8(2):127-30. PubMed ID: 17455106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.
    Wieser R; Fritz B; Ullmann R; Müller I; Galhuber M; Storlazzi CT; Ramaswamy A; Christiansen H; Shimizu N; Rehder H
    Hum Mutat; 2005 Aug; 26(2):78-83. PubMed ID: 15957176
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication.
    Yu S; Cox K; Friend K; Smith S; Buchheim R; Bain S; Liebelt J; Thompson E; Bratkovic D
    Clin Genet; 2008 Feb; 73(2):160-4. PubMed ID: 18076674
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions.
    Uddin RK; Zhang Y; Siu VM; Fan YS; O'Reilly RL; Rao J; Singh SM
    BMC Med Genet; 2006 Mar; 7():18. PubMed ID: 16512914
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DiGeorge syndrome: new insights.
    Goldmuntz E
    Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].
    Xu ZF; Yi L; Mo XM; Hu Y; Wang DJ; Zhu RF; Jiang YZ; Wu X; Wu Z; Shen L; Zhang Y; Zhong XL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):250-5. PubMed ID: 16767657
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
    Weksberg R; Hughes S; Moldovan L; Bassett AS; Chow EW; Squire JA
    BMC Genomics; 2005 Dec; 6():180. PubMed ID: 16351727
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital microgastria and primary ciliary dyskinesia in a newborn with DiGeorge syndrome and 22q11.2 deletion.
    Filippi L; Serafini L; Fiorini P; Agostini E; Giovannucci Uzielli ML
    Eur J Pediatr Surg; 2008 Jun; 18(3):195-7. PubMed ID: 18493898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical variability of the 22q11.2 duplication syndrome.
    Wentzel C; Fernström M; Ohrner Y; Annerén G; Thuresson AC
    Eur J Med Genet; 2008; 51(6):501-10. PubMed ID: 18707033
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.