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Journal Abstract Search

229 related items for PubMed ID: 12836465

  • 1. Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.
    Vantrappen G, Rommel N, Swillen A, Cremers CW, Fryns JP, Devriendt K.
    Acta Otorhinolaryngol Belg; 2003; 57(2):101-6. PubMed ID: 12836465
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  • 2. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G, Rommel N, Devriendt K, Cremers CW, Feenstra L, Fryns JP.
    Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
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  • 3. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
    Morava E, Masszi G, Czakó M, Tóth G, Melegh B, Kosztolányi G.
    Orv Hetil; 2000 Aug 20; 141(34):1873-5. PubMed ID: 11006712
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  • 4. Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?
    Swillen A, Vandeputte L, Cracco J, Maes B, Ghesquière P, Devriendt K, Fryns JP.
    Child Neuropsychol; 1999 Dec 20; 5(4):230-41. PubMed ID: 10925707
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  • 7. Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome.
    Rommel N, Vantrappen G, Swillen A, Devriendt K, Feenstra L, Fryns JP.
    Genet Couns; 1999 Dec 20; 10(1):71-8. PubMed ID: 10191432
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  • 8. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH.
    Genet Couns; 1999 Dec 20; 10(1):11-24. PubMed ID: 10191425
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  • 9. Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G, Devriendt K, Swillen A, Rommel N, Vogels A, Eyskens B, Gewillig M, Feenstra L, Fryns JP.
    Genet Couns; 1999 Dec 20; 10(1):3-9. PubMed ID: 10191424
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  • 11. The deletions of 22q11--the Portuguese experience.
    Gaspar IM, Lourenço MT, Reis MI, Soares MA, Nogueira G, Ferreira F, Feijóo MJ.
    Genet Couns; 1999 Dec 20; 10(1):51-7. PubMed ID: 10191429
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  • 12. Velo-cardio-facial syndrome: a review of 120 patients.
    Goldberg R, Motzkin B, Marion R, Scambler PJ, Shprintzen RJ.
    Am J Med Genet; 1993 Feb 01; 45(3):313-9. PubMed ID: 8434617
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  • 13. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.
    Shprintzen RJ, Goldberg RB, Lewin ML, Sidoti EJ, Berkman MD, Argamaso RV, Young D.
    Cleft Palate J; 1978 Jan 01; 15(1):56-62. PubMed ID: 272242
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  • 14. Velo-cardio-facial syndrome: a distinctive behavioral phenotype.
    Shprintzen RJ.
    Ment Retard Dev Disabil Res Rev; 2000 Jan 01; 6(2):142-7. PubMed ID: 10899808
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  • 19. Behavior problems and personality aspects of 40 children with velo-cardio-facial syndrome.
    Heineman-de Boer JA, Van Haelst MJ, Cordia-de Haan M, Beemer FA.
    Genet Couns; 1999 Jan 01; 10(1):89-93. PubMed ID: 10191434
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  • 20. Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school age.
    Swillen A, Devriendt K, Ghesquière P, Fryns JP.
    Genet Couns; 2001 Jan 01; 12(4):309-17. PubMed ID: 11837599
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