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Journal Abstract Search

127 related items for PubMed ID: 11339381

  • 1. 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
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  • 2. 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
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  • 3. 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
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  • 6. 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 Jan; 3(1):56-60. PubMed ID: 11339379
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  • 11. Prevalence and parental origin in Tetralogy of Fallot associated with chromosome 22q11 microdeletion.
    Lu JH, Chung MY, Hwang B, Chien HP.
    Pediatrics; 1999 Jul; 104(1 Pt 1):87-90. PubMed ID: 10390265
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  • 16. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.
    van Engelen K, Topf A, Keavney BD, Goodship JA, van der Velde ET, Baars MJ, Snijder S, Moorman AF, Postma AV, Mulder BJ.
    Heart; 2010 Apr; 96(8):621-4. PubMed ID: 20357389
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  • 17. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon AP, Keeton BR, Temple IK, Dennis NR.
    J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
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  • 18. Familial absent pulmonary valve syndrome without deletions of chromosome 22q11.
    McElhinney DB, Hanley FL, Stanger P.
    Cardiol Young; 2000 Nov; 10(6):618-20. PubMed ID: 11117395
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  • 19. 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
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  • 20. Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot.
    Carli D, Moroni A, Eleonora DG, Zonta A, Montin D, Licciardi F, Aidala E, Bordese R, Carlo PN, Brusco A, Giovanni Battista F, Mussa A.
    J Genet; 2021 Nov; 100():. PubMed ID: 33707356
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