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Journal Abstract Search

104 related items for PubMed ID: 8773902

  • 1. The search for hemizygosity at 22qll in patients with isolated cleft palate.
    Mingarelli R, Digilio MC, Mari A, Amati F, Standoli L, Giannotti A, Novelli G, Dallapiccola B.
    J Craniofac Genet Dev Biol; 1996; 16(2):118-21. PubMed ID: 8773902
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  • 2. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A.
    Am J Med Genet; 1995 Jul 03; 57(3):514-22. PubMed ID: 7677167
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  • 8. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
    Kelly D, Goldberg R, Wilson D, Lindsay E, Carey A, Goodship J, Burn J, Cross I, Shprintzen RJ, Scambler PJ.
    Am J Med Genet; 1993 Feb 01; 45(3):308-12. PubMed ID: 8434616
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  • 9. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M, Malkoç N, Ceviz N, Ozme S, Uludoğan S, Tunçbilek E.
    Turk J Pediatr; 2000 Feb 01; 42(3):215-8. PubMed ID: 11105620
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  • 13. Is isolated palatal anomaly an indication to screen for 22q11 region deletion?
    Reish O, Finkelstein Y, Mesterman R, Nachmani A, Wolach B, Fejgin M, Amiel A.
    Cleft Palate Craniofac J; 2003 Mar 01; 40(2):176-9. PubMed ID: 12605524
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  • 14. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
    Ford LC, Sulprizio SL, Rasgon BM.
    Laryngoscope; 2000 Mar 01; 110(3 Pt 1):362-7. PubMed ID: 10718420
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  • 15. Velocardiofacial manifestations and microdeletions in schizophrenic inpatients.
    Gothelf D, Frisch A, Munitz H, Rockah R, Aviram A, Mozes T, Birger M, Weizman A, Frydman M.
    Am J Med Genet; 1997 Nov 12; 72(4):455-61. PubMed ID: 9375731
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  • 16. 22q11 Deletion in children with cleft lip and palate--is routine screening justified?
    Bashir MA, Hodgkinson PD, Montgomery T, Splitt M.
    J Plast Reconstr Aesthet Surg; 2008 Nov 12; 61(2):130-2. PubMed ID: 17707704
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  • 20. Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency.
    Zori RT, Boyar FZ, Williams WN, Gray BA, Bent-Williams A, Stalker HJ, Rimer LA, Nackashi JA, Driscoll DJ, Rasmussen SA, Dixon-Wood V, Williams CA.
    Am J Med Genet; 1998 Apr 28; 77(1):8-11. PubMed ID: 9557885
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