BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 18160230)

  • 1. [Risk of missed diagnosis of 22q11.2 deletion in a fetal cardiac conotruncal malformation when another chromosomal abnormality is detected].
    Picone O; Brisset S; Senat MV; Maurin ML; Frydman R; Tachdjian G
    J Gynecol Obstet Biol Reprod (Paris); 2008 May; 37(3):299-301. PubMed ID: 18160230
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Microdeletion of 22q11 and conotruncal cardiopathies: contribution of prenatal diagnosis].
    Verspyck E; Joly G; Rossi A; David N; Blaysat G; Henocq A; Moirot H; Labadie G; Marpeau L
    J Gynecol Obstet Biol Reprod (Paris); 1999 Oct; 28(6):534-7. PubMed ID: 10598346
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
    Carotti A; Digilio MC; Piacentini G; Saffirio C; Di Donato RM; Marino B
    Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of a 22q11 deletion in a second-trimester fetus with conotruncal anomaly, absent thymus and meningomyelocele: Kousseff syndrome.
    Canda MT; Demir N; Bal FU; Doganay L; Sezer O
    J Obstet Gynaecol Res; 2012 Apr; 38(4):737-40. PubMed ID: 22380655
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [22q11 deletion in conotruncal anomalies].
    Kádár K
    Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
    Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital cardiac defects with 22q11 deletion.
    Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D
    Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
    López I; Bafalliu JA; Bernabé MC; García F; Costa M; Guillén-Navarro E
    Prenat Diagn; 2006 Jun; 26(6):577-80. PubMed ID: 16700088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of 22q11 microdeletion.
    Levy-Mozziconacci A; Piquet C; Heurtevin PC; Philip N
    Prenat Diagn; 1997 Nov; 17(11):1033-7. PubMed ID: 9399351
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.
    Boudjemline Y; Fermont L; Le Bidois J; Lyonnet S; Sidi D; Bonnet D
    J Pediatr; 2001 Apr; 138(4):520-4. PubMed ID: 11295715
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Use of amniocytes for prenatal diagnosis of 22q11.2 microdeletion syndrome: a feasibility study.
    Liu T; Liu Q; Wang YX; Yang D; Xin Y; Fang Z; Ding SF; Yang JF
    Chin Med J (Engl); 2010 Feb; 123(4):438-42. PubMed ID: 20193483
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population.
    Kong CW; Cheng YKY; To WWK; Leung TY
    Hong Kong Med J; 2019 Feb; 25(1):6-12. PubMed ID: 30655461
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Frequency of 22q11 deletions in children with isolated conotruncal defects].
    Shen L; Xu YJ; Zhao PJ; Sun K
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jan; 11(1):25-8. PubMed ID: 19149917
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 22q11.2 deletion mosaicism in patients with conotruncal heart defects.
    Jianrong L; Yinglong L; Xiaodong L; Cuntao Y; Bin C; Bo W
    Birth Defects Res A Clin Mol Teratol; 2006 Apr; 76(4):262-5. PubMed ID: 16575883
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatally diagnosed fetal lung lesions with associated conotruncal heart defects: is there a genetic association?
    Hüsler MR; Wilson RD; Rychik J; Bebbington MW; Johnson MP; Mann SE; Hedrick HL; Adzick S
    Prenat Diagn; 2007 Dec; 27(12):1123-8. PubMed ID: 17787025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review.
    Agergaard P; Hebert A; Sørensen KM; Østergaard JR; Olesen C
    Eur J Med Genet; 2011; 54(1):3-8. PubMed ID: 20965293
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of 22q11 microdeletion in a fetus with a conotruncal heart defect.
    Paladini D; Pacileo G; Palmieri S; Russo MG; Conti A; Piccola BD; Martinelli P
    Ultrasound Obstet Gynecol; 1998 Jan; 11(1):68-70. PubMed ID: 9511201
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.