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Journal Abstract Search

114 related items for PubMed ID: 17515164

  • 21. 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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  • 22. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
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  • 24. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.
    Amati F, Mari A, Digilio MC, Mingarelli R, Marino B, Giannotti A, Novelli G, Dallapiccola B.
    Hum Genet; 1995 May; 95(5):479-82. PubMed ID: 7759065
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  • 25. Tetralogy of Fallot in a patient with Killian-Pallister syndrome.
    Grech V, Parascandalo R, Cuschieri A.
    Pediatr Cardiol; 1999 May; 20(2):134-5. PubMed ID: 9986890
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  • 26. [22q11 deletion in conotruncal anomalies].
    Kádár K.
    Orv Hetil; 2005 Feb 20; 146(8):363-6. PubMed ID: 15803887
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  • 30. Intractable diarrhea with serious tetany in "CATCH 22".
    Nakagawa M, Okamoto N, Matsui A, Okagawa H, Kondoh M, Okuno M.
    J Pediatr Gastroenterol Nutr; 1998 Aug 20; 27(2):222-3. PubMed ID: 9702658
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  • 32. Can we predict 22q11 status of fetuses with tetralogy of Fallot?
    Boudjemline Y, Fermont L, Le Bidois J, Villain E, Sidi D, Bonnet D.
    Prenat Diagn; 2002 Mar 20; 22(3):231-4. PubMed ID: 11920900
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  • 33. Tetralogy of Fallot associated with pulmonary atresia and major aortopulmonary collateral arteries in a patient with interstitial deletion of 16q21-q22.1.
    Yamamoto T, Dowa Y, Ueda H, Kawataki M, Asou T, Sasaki Y, Harada N, Matsumoto N, Matsuoka R, Kurosawa K.
    Am J Med Genet A; 2008 Jun 15; 146A(12):1575-80. PubMed ID: 18470894
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  • 35. Isolated innominate artery in 22q11 microdeletion.
    Duke C, Chan KC.
    Pediatr Cardiol; 2001 Jun 15; 22(1):80-2. PubMed ID: 11123139
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  • 36. Asymmetric crying facies: a possible marker for congenital malformations.
    Rioja-Mazza D, Lieber E, Kamath V, Kalpatthi R.
    J Matern Fetal Neonatal Med; 2005 Oct 15; 18(4):275-7. PubMed ID: 16318980
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  • 38. Familial deletion of 22q11.2.
    Rodríguez Criado G, Gruesomontero J, Delicado Navarro A.
    Genet Couns; 1999 Oct 15; 10(3):325-7. PubMed ID: 10546107
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  • 39. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
    Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J.
    J Med Genet; 1993 Oct 15; 30(10):822-4. PubMed ID: 8230157
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  • 40. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B.
    J Med Genet; 1999 Feb 15; 36(2):137-9. PubMed ID: 10051013
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