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Journal Abstract Search

235 related items for PubMed ID: 12610907

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  • 3. [3 children with velocardiofacial (Shprintzen) syndrome].
    Lie DA, Beemer FA.
    Ned Tijdschr Geneeskd; 1996 Feb 17; 140(7):372-5. PubMed ID: 8628424
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  • 4. 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 Feb 17; 55(1):43-8. PubMed ID: 11256191
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  • 5. Surgical management of velopharyngeal incompetence in velocardiofacial syndrome.
    Mehendale FV, Birch MJ, Birkett L, Sell D, Sommerlad BC.
    Cleft Palate Craniofac J; 2004 Mar 17; 41(2):124-35. PubMed ID: 14989693
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  • 8. 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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  • 9. [Syndromes 3. Velo-cardio-facial (VCF/Shprintzen) syndrome].
    Beemer FA.
    Ned Tijdschr Tandheelkd; 1998 Aug 23; 105(8):287-8. PubMed ID: 11928434
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  • 11. CATCH 22.
    Hall JG.
    J Med Genet; 1993 Oct 23; 30(10):801-2. PubMed ID: 8230153
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  • 13. Velocardiofacial syndrome associated with atrophy of the shoulder girdle muscles and cervicomedullary narrowing.
    Bolland E, Manzur AY, Milward TM, Muntoni F.
    Eur J Paediatr Neurol; 2000 Oct 23; 4(2):73-6. PubMed ID: 10817488
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  • 14. Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype.
    Holder SE, Winter RM, Kamath S, Scambler PJ.
    J Med Genet; 1993 Oct 23; 30(10):825-7. PubMed ID: 8230158
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  • 15. Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).
    Antshel KM, Conchelos J, Lanzetta G, Fremont W, Kates WR.
    Psychiatry Res; 2005 Apr 30; 138(3):235-45. PubMed ID: 15854791
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  • 17. Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome.
    Bearden CE, Wang PP, Simon TJ.
    Am J Med Genet; 2002 Aug 08; 114(6):689-92. PubMed ID: 12210289
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  • 19. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G, Bartmus D, Bartels I.
    Genet Couns; 1998 Aug 08; 9(3):223-7. PubMed ID: 9777346
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  • 20. Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?
    Eliez S, Blasey CM, Schmitt EJ, White CD, Hu D, Reiss AL.
    Am J Psychiatry; 2001 Mar 08; 158(3):447-53. PubMed ID: 11229987
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