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Journal Abstract Search

152 related items for PubMed ID: 7243440

  • 1. Familial third and fourth pharyngeal pouch syndrome with truncus arteriosus: DiGeorge syndrome.
    Raatikka M, Rapola J, Tuuteri L, Louhimo I, Savilahti E.
    Pediatrics; 1981 Feb; 67(2):173-5. PubMed ID: 7243440
    [Abstract] [Full Text] [Related]

  • 2. Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission.
    Rohn RD, Leffell MS, Leadem P, Johnson D, Rubio T, Emanuel BS.
    J Pediatr; 1984 Jul; 105(1):47-51. PubMed ID: 6737148
    [Abstract] [Full Text] [Related]

  • 3. Familial truncus arteriosus: a possible autosomal-recessive trait.
    Abushaban L, Uthaman B, Kumar AR, Selvan J.
    Pediatr Cardiol; 2003 Jul; 24(1):64-6. PubMed ID: 12574981
    [Abstract] [Full Text] [Related]

  • 4. [Truncus arteriosus: an autosomal recessive disease?].
    le Marec B, Odent S, Almange C, Journel H, Roussey M, Defawe G.
    J Genet Hum; 1989 Sep; 37(3):225-30. PubMed ID: 2625625
    [Abstract] [Full Text] [Related]

  • 5. Di George anomaly and velocardiofacial syndrome.
    Stevens CA, Carey JC, Shigeoka AO.
    Pediatrics; 1990 Apr; 85(4):526-30. PubMed ID: 2314965
    [Abstract] [Full Text] [Related]

  • 6. Selective polysaccharide antibody deficiency in familial DiGeorge syndrome.
    Schubert MS, Moss RB.
    Ann Allergy; 1992 Sep; 69(3):231-8. PubMed ID: 1524280
    [Abstract] [Full Text] [Related]

  • 7. Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature.
    Dallapiccola B, Marino B, Giannotti A, Valorani G.
    Ann Genet; 1989 Sep; 32(2):92-6. PubMed ID: 2667458
    [Abstract] [Full Text] [Related]

  • 8. Neonate with dysmorphic facies and heart defects.
    Conley ME, Lillie MA.
    Hosp Pract (Off Ed); 1981 Sep; 16(9):100, 104. PubMed ID: 6792035
    [No Abstract] [Full Text] [Related]

  • 9. DiGeorge syndrome presenting as severe congenital heart disease in the newborn.
    Finley JP, Collins GF, de Chadarévian JP, Williams RL.
    Can Med Assoc J; 1977 Mar 19; 116(6):635-40. PubMed ID: 608163
    [Abstract] [Full Text] [Related]

  • 10. Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.
    Van Mierop LH, Kutsche LM.
    Am J Cardiol; 1986 Jul 01; 58(1):133-7. PubMed ID: 3728313
    [Abstract] [Full Text] [Related]

  • 11. The teratogenic effects of a bis(dichloroacetyl)diamine on hamster embryos. Aortic arch anomalies and the pathogenesis of the DiGeorge syndrome.
    Binder M.
    Am J Pathol; 1985 Feb 01; 118(2):179-93. PubMed ID: 3970137
    [Abstract] [Full Text] [Related]

  • 12. DiGeorge syndrome with truncus arteriosus: report of one case.
    Liang PH, Chen MR, Shyur SD, Lee YJ, Lin SP, Yu MT, Chiu IS, Chen SJ.
    Acta Paediatr Taiwan; 2004 Feb 01; 45(3):174-7. PubMed ID: 15493739
    [Abstract] [Full Text] [Related]

  • 13. Congenital microgastria and primary ciliary dyskinesia in a newborn with DiGeorge syndrome and 22q11.2 deletion.
    Filippi L, Serafini L, Fiorini P, Agostini E, Giovannucci Uzielli ML.
    Eur J Pediatr Surg; 2008 Jun 01; 18(3):195-7. PubMed ID: 18493898
    [Abstract] [Full Text] [Related]

  • 14. Truncus arteriosus communis associated with chromosome 22q11 deletion.
    Momma K, Ando M, Matsuoka R.
    J Am Coll Cardiol; 1997 Oct 01; 30(4):1067-71. PubMed ID: 9316541
    [Abstract] [Full Text] [Related]

  • 15. Familial DiGeorge syndrome and associated partial monosomy of chromosome 22.
    Greenberg F, Crowder WE, Paschall V, Colon-Linares J, Lubianski B, Ledbetter DH.
    Hum Genet; 1984 Oct 01; 65(4):317-9. PubMed ID: 6693120
    [Abstract] [Full Text] [Related]

  • 16. Genetics of conotruncal malformations: further evidence of autosomal recessive inheritance.
    Rein AJ, Sheffer R.
    Am J Med Genet; 1994 Apr 15; 50(3):302-3. PubMed ID: 8042678
    [No Abstract] [Full Text] [Related]

  • 17. Spectrum of Di George syndrome in patients with truncus arteriosus: expanded Di George syndrome.
    Radford DJ, Perkins L, Lachman R, Thong YH.
    Pediatr Cardiol; 1988 Apr 15; 9(2):95-101. PubMed ID: 3399433
    [Abstract] [Full Text] [Related]

  • 18. Human Genetics of Truncus Arteriosus.
    Yamagishi H.
    Adv Exp Med Biol; 2024 Apr 15; 1441():841-852. PubMed ID: 38884753
    [Abstract] [Full Text] [Related]

  • 19. ENU induced mutations causing congenital cardiovascular anomalies.
    Yu Q, Shen Y, Chatterjee B, Siegfried BH, Leatherbury L, Rosenthal J, Lucas JF, Wessels A, Spurney CF, Wu YJ, Kirby ML, Svenson K, Lo CW.
    Development; 2004 Dec 15; 131(24):6211-23. PubMed ID: 15548583
    [Abstract] [Full Text] [Related]

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