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 *

119 related articles for article (PubMed ID: 1425789)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?
    Farag TI; Teebi AS
    Am J Med Genet; 1990 Apr; 35(4):516-8. PubMed ID: 2333881
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tetralogy of Fallot with pulmonary atresia in siblings.
    Der Kaloustian VM; Ratl H; Malouf J; Hatem J; Slim M; Tomeh A; Khouri J; Kutayli F
    Am J Med Genet; 1985 May; 21(1):119-22. PubMed ID: 4003436
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
    Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G
    Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unusual retinal abnormalities in sisters with tetralogy of Fallot.
    Zanolli MT; Capasso J; Khetan V; Aristimuño B; Levin AV
    J AAPOS; 2014 Dec; 18(6):601-4. PubMed ID: 25448148
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
    El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S
    Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.
    Huang RT; Wang J; Xue S; Qiu XB; Shi HY; Li RG; Qu XK; Yang XX; Liu H; Li N; Li YJ; Xu YJ; Yang YQ
    Int J Med Sci; 2017; 14(4):323-332. PubMed ID: 28553164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Asplenia syndrome with congenital heart disease and tetralogy of Fallot in siblings.
    Silver W; Steier M; Chandra N
    Am J Cardiol; 1972 Jul; 30(1):91-4. PubMed ID: 5035578
    [No Abstract]   [Full Text] [Related]  

  • 16. [Tetralogy of Fallot in monozygotic twins].
    Laugel V; Livolsi A; Viville B; Langer B; Messer J; Fischbach M
    Arch Pediatr; 2001 Apr; 8(4):385-8. PubMed ID: 11339130
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diagnosis of familial Holt-Oram syndrome].
    Lehner R; Wenzl R; Vanura H; Frank W; Safar P; Husslein P
    Z Geburtshilfe Perinatol; 1994 Aug; 198(4):143-9. PubMed ID: 7975801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tetralogy of Fallot in three sibs.
    Pankau R; Siekmeyer W; Stoffregen R
    Am J Med Genet; 1990 Dec; 37(4):532-3. PubMed ID: 2260602
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.
    Grunert M; Dorn C; Schueler M; Dunkel I; Schlesinger J; Mebus S; Alexi-Meskishvili V; Perrot A; Wassilew K; Timmermann B; Hetzer R; Berger F; Sperling SR
    Hum Mol Genet; 2014 Jun; 23(12):3115-28. PubMed ID: 24459294
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital heart disease among the hutterite brethren.
    Lee RV; Buker RS
    N Engl J Med; 1969 May; 280(19):1061-2. PubMed ID: 5778414
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.