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Journal Abstract Search

264 related items for PubMed ID: 6264787

  • 1. Multiple congenital anomalies, thymic dysplasia, severe congenital heart disease, and oligosyndactyly with a deletion of the short arm of chromosome 5.
    Taylor MJ, Josifek K.
    Am J Med Genet; 1981; 9(1):5-11. PubMed ID: 6264787
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  • 2. 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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  • 5. Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence.
    Mascarello JT, Bastian JF, Jones MC.
    Am J Med Genet; 1989 Jan; 32(1):112-4. PubMed ID: 2705472
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  • 6. CATCHing a break on 22.
    Glover TW.
    Nat Genet; 1995 Jul; 10(3):257-8. PubMed ID: 7670460
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  • 9. DiGeorge anomaly in an infant with deletion of chromosome 22 and dup(9p) due to adjacent type II disjunction.
    el-Fouly MH, Higgins JV, Kapur S, Sankey BJ, Matisoff DN, Costa-Fox M.
    Am J Med Genet; 1991 Mar 15; 38(4):569-73. PubMed ID: 2063901
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  • 11. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
    Carotti A, Digilio MC, Piacentini G, Saffirio C, Di Donato RM, Marino B.
    Dev Disabil Res Rev; 2008 Mar 15; 14(1):35-42. PubMed ID: 18636635
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  • 12. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
    Wulfsberg EA.
    Am J Med Genet; 1996 Aug 23; 64(3):523-4. PubMed ID: 8862634
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  • 17. 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
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  • 19. Heart disease associated with deletion of the short arm of chromosome 18.
    Movahhedian HR, Kane HA, Borgaonkar D, McDermott M, Septimus S.
    Del Med J; 1991 May 19; 63(5):285-9. PubMed ID: 1860515
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