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 *

145 related articles for article (PubMed ID: 7677092)

  • 1. Tetralogy of Fallot associated with chromosome 22q11 deletion.
    Momma K; Kondo C; Ando M; Matsuoka R; Takao A
    Am J Cardiol; 1995 Sep; 76(8):618-21. PubMed ID: 7677092
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
    Burn J; Takao A; Wilson D; Cross I; Momma K; Wadey R; Scambler P; Goodship J
    J Med Genet; 1993 Oct; 30(10):822-4. PubMed ID: 8230157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.
    Oh DC; Min JY; Lee MH; Kim YM; Park SY; Won HS; Kim IK; Lee YH; Yoo SJ; Ryu HM
    J Korean Med Sci; 2002 Feb; 17(1):125-8. PubMed ID: 11850602
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome 22q11 microdeletions in tetralogy of Fallot.
    Trainer AH; Morrison N; Dunlop A; Wilson N; Tolmie J
    Arch Dis Child; 1996 Jan; 74(1):62-3. PubMed ID: 8660052
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Towards earlier diagnosis of 22q11 deletions.
    Tobias ES; Morrison N; Whiteford ML; Tolmie JL
    Arch Dis Child; 1999 Dec; 81(6):513-4. PubMed ID: 10569971
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
    Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
    Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial deletion of 22q11.2.
    Rodríguez Criado G; Gruesomontero J; Delicado Navarro A
    Genet Couns; 1999; 10(3):325-7. PubMed ID: 10546107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 22q11.2 microdeletions in adults with familial tetralogy of Fallot.
    Hokanson JS; Pierpont E; Hirsch B; Moller JH
    Genet Med; 2001; 3(1):61-4. PubMed ID: 11339381
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequent association of 22q11.2 deletion with tetralogy of Fallot.
    Maeda J; Yamagishi H; Matsuoka R; Ishihara J; Tokumura M; Fukushima H; Ueda H; Takahashi E; Yoshiba S; Kojima Y
    Am J Med Genet; 2000 Jun; 92(4):269-72. PubMed ID: 10842294
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Study on the relationship between 22q11 microdeletion and congenital heart disease].
    Du YR; Yang HJ; Tan Z; Huang Y; Li SL; Tian JW; Zhang GY; Li P; Fu SB
    Yi Chuan; 2005 Nov; 27(6):873-6. PubMed ID: 16378931
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults.
    Momma K; Takao A; Matsuoka R; Imai Y; Muto A; Osawa M; Takayama M
    Genet Med; 2001; 3(1):56-60. PubMed ID: 11339379
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Influence of chromosome 22q11.2 microdeletion on surgical outcome after treatment of tetralogy of fallot with pulmonary atresia.
    Carotti A; Marino B; Di Donato RM
    J Thorac Cardiovasc Surg; 2003 Nov; 126(5):1666-7. PubMed ID: 14666061
    [No Abstract]   [Full Text] [Related]  

  • 14. Counseling families with chromosome 22q11 deletions: the catch in CATCH-22.
    Bristow JD; Bernstein HS
    J Am Coll Cardiol; 1998 Aug; 32(2):499-501. PubMed ID: 9708482
    [No Abstract]   [Full Text] [Related]  

  • 15. Mosaic 22q11.2 deletion and tetralogy of Fallot with absent pulmonary valve: an unreported association.
    Prabhu S; Jenny B; James H; Provenzano S
    World J Pediatr Congenit Heart Surg; 2015 Apr; 6(2):342-5. PubMed ID: 25870364
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
    Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
    Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exclusion of 22q11 deletion in Noonan syndrome with tetralogy of Fallot.
    Digilio MC; Marino B; Giannotti A; Dallapiccola B
    Am J Med Genet; 1996 Apr; 62(4):413-4. PubMed ID: 8723074
    [No Abstract]   [Full Text] [Related]  

  • 19. [Chromosome 22q11.2 microdeletion and phenotype analysis of patients with non-syndromic tetralogy of Fallot].
    Zhang ZW; Deng JY; Ying LY; Gao Z; Jin J; Qi JC; Tan Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):708-11. PubMed ID: 22161111
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.
    Amati F; Mari A; Digilio MC; Mingarelli R; Marino B; Giannotti A; Novelli G; Dallapiccola B
    Hum Genet; 1995 May; 95(5):479-82. PubMed ID: 7759065
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.