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 *

75 related articles for article (PubMed ID: 7399662)

  • 1. Tetralogy of Fallot and alkaptonuria in successive generations.
    Haiya PP; Balaji NK; Sukumar IP; Cherian G
    Indian Pediatr; 1980 Jan; 17(1):83-5. PubMed ID: 7399662
    [No Abstract]   [Full Text] [Related]  

  • 2. Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of Fallot.
    Vergara P; Digilio MC; De Zorzi A; Di Carlo D; Capolino R; Rimini A; Pelegrini M; Calabro R; Marino B
    Clin Dysmorphol; 2006 Apr; 15(2):65-70. PubMed ID: 16531730
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tetralogy of Fallot in monozygotic twins.
    Patel AB; Renge RL
    Indian Heart J; 2002; 54(1):83-5. PubMed ID: 11999095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Polymorphism C242T of the gene of the p22phox subunit for nicotinamide adenine dinucleotide phosphate oxidase, and erythrocytic antioxidant enzymes, in patients with tetralogy of Fallot.
    Guerra A; Rego C; Coelho C; Guimarães N; Thiran C; Aguiar A; Areias JC; Bicho M
    Cardiol Young; 2007 Jun; 17(3):295-300. PubMed ID: 17445342
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Smith-Magenis syndrome and tetralogy of Fallot.
    Sweeney E; Peart I; Tofeig M; Kerr B
    J Med Genet; 1999 Jun; 36(6):501-2. PubMed ID: 10874646
    [No Abstract]   [Full Text] [Related]  

  • 7. Type III tracheal agenesis with familial tetralogy of Fallot and absent pulmonary valve syndrome.
    Hirt-Armon K; Pober BR; Holmes LB
    Am J Med Genet; 1996 Nov; 65(4):266-8. PubMed ID: 8923932
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The methylenetetrahydrofolate reductase gene variant (C677T) as a susceptibility gene for tetralogy of Fallot.
    Marinho C; Alho I; Guerra A; Rego C; Areias J; Bicho M
    Rev Port Cardiol; 2009; 28(7-8):809-12. PubMed ID: 19894660
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cerebrovascular events in young adults after surgical repair of tetralogy of Fallot.
    Chow CK; Amos D; Celermajer DS
    Cardiol Young; 2005 Apr; 15(2):130-2. PubMed ID: 15845154
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Correction of tetralogy of Fallot in patients with a single pulmonary artery].
    Liu JS; Wang ZW
    Zhonghua Wai Ke Za Zhi; 1994 Mar; 32(3):172-4. PubMed ID: 7842910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Long-term outcome of surgically treated teratology of Fallot].
    Ben Khalfallah A; Annabi N; Ousji M
    Tunis Med; 2004 Jan; 82 Suppl 1():88-93. PubMed ID: 15127696
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.
    Pizzuti A; Sarkozy A; Newton AL; Conti E; Flex E; Digilio MC; Amati F; Gianni D; Tandoi C; Marino B; Crossley M; Dallapiccola B
    Hum Mutat; 2003 Nov; 22(5):372-7. PubMed ID: 14517948
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Etiology and incidence of tetralogy of Fallot].
    Bakhtina GG; Shurgaia AM
    Pediatriia; 1973 Dec; 52(12):40. PubMed ID: 4786421
    [No Abstract]   [Full Text] [Related]  

  • 14. Pulmonary valve replacement late after repair of tetralogy of Fallot.
    Yemets IM; Williams WG; Webb GD; Harrison DA; McLaughlin PR; Trusler GA; Coles JG; Rebeyka IM; Freedom RM
    Ann Thorac Surg; 1997 Aug; 64(2):526-30. PubMed ID: 9262606
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
    Pollak MR; Chou YH; Cerda JJ; Steinmann B; La Du BN; Seidman JG; Seidman CE
    Nat Genet; 1993 Oct; 5(2):201-4. PubMed ID: 8252048
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A familial disorder with duodenal atresia and tetralogy of Fallot.
    Lemire EG; Evans JA; Giddins NG; Harman CR; Wiseman NE; Chudley AE
    Am J Med Genet; 1996 Dec; 66(1):39-44. PubMed ID: 8957509
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparison between QRS duration at standard ECG and signal-averaging ECG for arrhythmic risk stratification after surgical repair of tetralogy of fallot.
    Russo G; Folino AF; Mazzotti E; Rebellato L; Daliento L
    J Cardiovasc Electrophysiol; 2005 Mar; 16(3):288-92. PubMed ID: 15817088
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Surgical correction of tetralogy of Fallot with unilateral absence of pulmonary artery.
    Bockeria LA; Podzolkov VP; Makhachev OA; Zelenikin MA; Alekian BG; Ilyin VN; Gadjiev AA; Shatalov KV; Kakuchaya TT; Khiriev TKh; Zaets SB
    Ann Thorac Surg; 2007 Feb; 83(2):613-8. PubMed ID: 17257996
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reoperation for tricuspid regurgitation after total correction of tetralogy of Fallot.
    Hachiro Y; Takagi N; Koyanagi T; Abe T
    Ann Thorac Cardiovasc Surg; 2002 Aug; 8(4):199-203. PubMed ID: 12472382
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.