These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

926 related articles for article (PubMed ID: 9951451)

  • 1. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA; Hatchwell E; Barber JC; Daubeney PE; Crolla JA; Salmon AP; Keeton BR; Temple IK; Dennis NR
    J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
    Ziolkowska L; Kawalec W; Turska-Kmiec A; Krajewska-Walasek M; Brzezinska-Rajszys G; Daszkowska J; Maruszewski B; Burczynski P
    Eur J Pediatr; 2008 Oct; 167(10):1135-40. PubMed ID: 18172682
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?
    Rauch R; Rauch A; Koch A; Zink S; Kaulitz R; Girisch M; Singer H; Hofbeck M
    Eur J Pediatr; 2004 Nov; 163(11):642-5. PubMed ID: 15300432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
    Iserin L; de Lonlay P; Viot G; Sidi D; Kachaner J; Munnich A; Lyonnet S; Vekemans M; Bonnet D
    Eur J Pediatr; 1998 Nov; 157(11):881-4. PubMed ID: 9835429
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB; Chen E; Golabi M; Lebo RV
    Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K; Kondo C; Matsuoka R
    J Am Coll Cardiol; 1996 Jan; 27(1):198-202. PubMed ID: 8522695
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microdeletion 22q11 in complex cardiovascular malformations.
    Mehraein Y; Wippermann CF; Michel-Behnke I; Nhan Ngo TK; Hillig U; Giersberg M; Aulepp U; Barth H; Fritz B; Rehder H
    Hum Genet; 1997 Apr; 99(4):433-42. PubMed ID: 9099830
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients.
    Borgmann S; Luhmer I; Arslan-Kirchner M; Kallfelz HC; Schmidtke J
    Eur J Pediatr; 1999 Dec; 158(12):958-63. PubMed ID: 10592069
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [22q11.2 deletion syndrome and complex congenital heart defects].
    Rosa RF; Trevisan P; Koshiyama DB; Pilla CB; Zen PR; Varella-Garcia M; Paskulin GA
    Rev Assoc Med Bras (1992); 2011; 57(1):62-5. PubMed ID: 21390462
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Anatomic patterns of conotruncal defects associated with deletion 22q11.
    Marino B; Digilio MC; Toscano A; Anaclerio S; Giannotti A; Feltri C; de Ioris MA; Angioni A; Dallapiccola B
    Genet Med; 2001; 3(1):45-8. PubMed ID: 11339377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tricuspid atresia and 22q11 deletion.
    Marino B; Digilio MC; Novelli G; Giannotti A; Dallapiccola B
    Am J Med Genet; 1997 Oct; 72(1):40-2. PubMed ID: 9295072
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal abnormalities among children born with conotruncal cardiac defects.
    Lammer EJ; Chak JS; Iovannisci DM; Schultz K; Osoegawa K; Yang W; Carmichael SL; Shaw GM
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
    Wozniak A; Wolnik-Brzozowska D; Wisniewska M; Glazar R; Materna-Kiryluk A; Moszura T; Badura-Stronka M; Skolozdrzy J; Krawczynski MR; Zeyland J; Bobkowski W; Slomski R; Latos-Bielenska A; Siwinska A
    BMC Pediatr; 2010 Dec; 10():88. PubMed ID: 21134246
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.
    Takahashi K; Kido S; Hoshino K; Ogawa K; Ohashi H; Fukushima Y
    Eur J Pediatr; 1995 Nov; 154(11):878-81. PubMed ID: 8582397
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 47.