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 *

96 related articles for article (PubMed ID: 10931419)

  • 1. Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome.
    Hopkin RJ; Schorry EK; Bofinger M; Saal HM
    J Pediatr; 2000 Aug; 137(2):247-9. PubMed ID: 10931419
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
    Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G; Bartmus D; Bartels I
    Genet Couns; 1998; 9(3):223-7. PubMed ID: 9777346
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A
    In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype.
    Giannotti A; Digilio MC; Marino B; Mingarelli R; Dallapiccola B
    Am J Med Genet; 1994 Nov; 53(3):303-4. PubMed ID: 7856669
    [No Abstract]   [Full Text] [Related]  

  • 8. [CATCH-22: a microdeletion of chromosome 22 behind the polymorphous syndrome].
    Somer M; Ignatius J; Vehmanen P; Keinänen M; Haapanen ML
    Duodecim; 1997; 113(12):1115-22. PubMed ID: 11466836
    [No Abstract]   [Full Text] [Related]  

  • 9. Scoliosis in velo-cardio-facial syndrome.
    Morava E; Lacassie Y; King A; Illes T; Marble M
    J Pediatr Orthop; 2002; 22(6):780-3. PubMed ID: 12409907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
    Park IS; Ko JK; Kim YH; Yoo HW; Seo EJ; Choi JY; Gil HY; Kim SJ
    Int J Cardiol; 2007 Jan; 114(2):230-5. PubMed ID: 16824627
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The 22q11.2 deletion syndrome.
    Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
    Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome.
    Bearden CE; Wang PP; Simon TJ
    Am J Med Genet; 2002 Aug; 114(6):689-92. PubMed ID: 12210289
    [No Abstract]   [Full Text] [Related]  

  • 14. Avoiding perils and pitfalls in velocardiofacial syndrome: an otolaryngologist's perspective.
    Cable BB; Mair EA
    Ear Nose Throat J; 2003 Jan; 82(1):56-60. PubMed ID: 12610907
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differential detection of deletion 22q11.2 syndrome by specialty and indication.
    Katzman PJ; Wang B; Sawhney M; Wang N
    Pediatr Dev Pathol; 2005; 8(5):557-67. PubMed ID: 16222476
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [22q11 deletion in conotruncal anomalies].
    Kádár K
    Orv Hetil; 2005 Feb; 146(8):363-6. PubMed ID: 15803887
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects.
    Michielon G; Marino B; Oricchio G; Digilio MC; Iorio F; Filippelli S; Placidi S; Di Donato RM
    J Thorac Cardiovasc Surg; 2009 Sep; 138(3):565-570.e2. PubMed ID: 19698836
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Associated anomalies in asymmetric crying facies and 22q11 deletion.
    Akcakus M; Ozkul Y; Gunes T; Kurtoglu S; Cetin N; Kisaarslan AP; Dundar M
    Genet Couns; 2003; 14(3):325-30. PubMed ID: 14577677
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Velocardiofacial syndrome (Shprintzen syndrome, chromosome 22q11 deletion syndrome).
    Olney AH; Kolodziej P
    Ear Nose Throat J; 1998 Jun; 77(6):460-1. PubMed ID: 9674319
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP
    Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.