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 *

112 related articles for article (PubMed ID: 1884513)

  • 1. The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot with pulmonary atresia.
    Wulfsberg EA; Zintz EJ; Moore JW
    Clin Genet; 1991 Jul; 40(1):12-6. PubMed ID: 1884513
    [TBL] [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. Clinical profile of patients with tetralogy of Fallot admitted for surgery at a cardiac surgical centre.
    Otaigbe BE; Kumar S
    JNMA J Nepal Med Assoc; 2011; 51(182):62-6. PubMed ID: 22916514
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis?
    Chassagnon G; Lefort B; Meot M; Carpentier E; Sirinelli D; Chantepie A; Morel B
    J Am Heart Assoc; 2017 Dec; 7(1):. PubMed ID: 29288155
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Conotruncal malformation complex: examples of possible monogenic inheritance.
    Miller ME; Smith DW
    Pediatrics; 1979 Jun; 63(6):890-3. PubMed ID: 450526
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age.
    Chin-Yee NJ; Costain G; Swaby JA; Silversides CK; Bassett AS
    Circ Cardiovasc Genet; 2014 Apr; 7(2):102-9. PubMed ID: 24563425
    [TBL] [Abstract][Full Text] [Related]  

  • 7. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease.
    Gelb BD; Towbin JA; McCabe ER; Sujansky E
    Am J Med Genet; 1991 Sep; 40(4):471-6. PubMed ID: 1746613
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tetralogy of Fallot in three siblings: a familial study and review of the literature.
    Pacileo G; Musewe NN; Calabrò R
    Eur J Pediatr; 1992 Oct; 151(10):726-7. PubMed ID: 1425789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complete atrioventricular canal associated with conotruncal malformations: anatomical observations in 13 specimens.
    Thiene G; Frescura C; Di Donato R; Gallucci V
    Eur J Cardiol; 1979 Mar; 9(3):199-213. PubMed ID: 421722
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetics of conotruncal malformations: further evidence of autosomal recessive inheritance.
    Rein AJ; Sheffer R
    Am J Med Genet; 1994 Apr; 50(3):302-3. PubMed ID: 8042678
    [No Abstract]   [Full Text] [Related]  

  • 11. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
    Beauchesne LM; Warnes CA; Connolly HM; Ammash NM; Grogan M; Jalal SM; Michels VV
    J Am Coll Cardiol; 2005 Feb; 45(4):595-8. PubMed ID: 15708709
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.
    Digilio MC; Marino B; Giannotti A; Toscano A; Dallapiccola B
    J Med Genet; 1997 Mar; 34(3):188-90. PubMed ID: 9132487
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.
    Digilio MC; Marino B; Grazioli S; Agostino D; Giannotti A; Dallapiccola B
    Am J Cardiol; 1996 Jun; 77(15):1375-6. PubMed ID: 8677886
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Elevated birth prevalence of conotruncal heart defects in a population with high consanguinity rate.
    Stavsky M; Robinson R; Sade MY; Krymko H; Zalstein E; Ioffe V; Novack V; Levitas A
    Cardiol Young; 2017 Jan; 27(1):109-116. PubMed ID: 26979327
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?
    Lammer EJ; Scholes T; Abrams L
    Clin Dysmorphol; 2001 Jan; 10(1):9-13. PubMed ID: 11152158
    [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. [Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].
    Buendía Hernández A; Calderón-Colmenero J; Aizpuru E; Attie CL; Zabal C; Patiño E; Miranda I; Juanico A; Attie F
    Arch Inst Cardiol Mex; 2000; 70(2):148-53. PubMed ID: 10932799
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Radiofrequency perforation in the treatment of acquired left pulmonary artery atresia following repair of tetralogy of Fallot.
    Kort HW; Balzer DT
    Catheter Cardiovasc Interv; 2003 Sep; 60(1):79-81. PubMed ID: 12929107
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial tetralogy of Fallot and glaucoma.
    Chen SC; D'Souza N
    Am J Med Genet; 1990 Sep; 37(1):40-1. PubMed ID: 2240041
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.