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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

151 related items for PubMed ID: 16854201

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  • 4. Presence of 22q11 deletion in postadenoidectomy velopharyngeal insufficiency.
    Perkins JA, Sie K, Gray S.
    Arch Otolaryngol Head Neck Surg; 2000 May; 126(5):645-8. PubMed ID: 10807333
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  • 7. Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome.
    Goldmuntz E, Driscoll DA, Emanuel BS, McDonald-McGinn D, Mei M, Zackai E, Mitchell LE.
    Birth Defects Res A Clin Mol Teratol; 2009 Feb; 85(2):125-9. PubMed ID: 18770859
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  • 8. 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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  • 10. Palatal evaluation and treatment in 22q11.2 deletion syndrome.
    Jackson O, Crowley TB, Sharkus R, Smith R, Jeong S, Solot C, McDonald-Mcginn D.
    Am J Med Genet A; 2019 Jul 28; 179(7):1184-1195. PubMed ID: 31038278
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  • 13. Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).
    Wang PP, Woodin MF, Kreps-Falk R, Moss EM.
    Dev Med Child Neurol; 2000 Jun 28; 42(6):422-7. PubMed ID: 10875531
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  • 18. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.
    Gerdes M, Solot C, Wang PP, Moss E, LaRossa D, Randall P, Goldmuntz E, Clark BJ, Driscoll DA, Jawad A, Emanuel BS, McDonald-McGinn DM, Batshaw ML, Zackai EH.
    Am J Med Genet; 1999 Jul 16; 85(2):127-33. PubMed ID: 10406665
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  • 19. 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 Jul 16; 55(1):43-8. PubMed ID: 11256191
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  • 20. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).
    McQuade L, Christodoulou J, Budarf M, Sachdev R, Wilson M, Emanuel B, Colley A.
    Am J Med Genet; 1999 Sep 03; 86(1):27-33. PubMed ID: 10440825
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