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Journal Abstract Search

190 related items for PubMed ID: 18654600

  • 1. 22q11.2 microdeletion syndrome is a common cause of renal tract malformations.
    Burtey S.
    Nat Clin Pract Nephrol; 2008 Aug; 4(8):E1. PubMed ID: 18654600
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  • 2. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome].
    Hjalgrim H, Hahnemann JM, Timshel S, Brøndum-Nielsen K.
    Ugeskr Laeger; 2000 Jul 31; 162(31):4169-70. PubMed ID: 10962926
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  • 10. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
    Sullivan KE.
    Immunol Allergy Clin North Am; 2008 May 31; 28(2):353-66. PubMed ID: 18424337
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  • 11. Renal malformations in deletion 22q11.2 patients.
    Kujat A, Schulz MD, Strenge S, Froster UG.
    Am J Med Genet A; 2006 Jul 15; 140(14):1601-2. PubMed ID: 16761295
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  • 12. 22q11.2 deletion syndrome: introduction.
    Lajiness-O'Neill R.
    Child Neuropsychol; 2005 Feb 15; 11(1):1-3. PubMed ID: 15823979
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  • 13. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
    Qin YF, Yang JB, Xie CH, Shao J, Zhao ZY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun 15; 24(3):284-7. PubMed ID: 17557238
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  • 18. 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. 22q11 deletion syndrome: is that what they used to call . . . ?
    Umlauf MG.
    Perspect Psychiatr Care; 2008 Oct 08; 44(4):259-66. PubMed ID: 18826464
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  • 20. Renal and urological tract malformations caused by a 22q11 deletion.
    Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M.
    J Med Genet; 1996 Apr 08; 33(4):349. PubMed ID: 8730297
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