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Journal Abstract Search

175 related items for PubMed ID: 18268261

  • 21. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
    Sullivan KE.
    Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
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  • 22. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.
    Shuib S, Abdul Latif Z, Abidin NZ, Akmal SN, Zakaria Z.
    Malays J Pathol; 2009 Dec; 31(2):133-6. PubMed ID: 20514857
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  • 25. Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases.
    Larson RS, Butler MG.
    Diagn Mol Pathol; 1995 Dec; 4(4):274-8. PubMed ID: 8634784
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  • 26. Primary amenorrhea and absent uterus in the 22q11.2 deletion syndrome.
    Sundaram UT, McDonald-McGinn DM, Huff D, Emanuel BS, Zackai EH, Driscoll DA, Bodurtha J.
    Am J Med Genet A; 2007 Sep 01; 143A(17):2016-8. PubMed ID: 17676598
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  • 33. FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.
    Yakut T, Kilic SS, Cil E, Yapici E, Egeli U.
    Pediatr Surg Int; 2006 Apr 01; 22(4):380-3. PubMed ID: 16463032
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  • 37. Ocular findings in the chromosome 22q11.2 deletion syndrome.
    Forbes BJ, Binenbaum G, Edmond JC, DeLarato N, McDonald-McGinn DM, Zackai EH.
    J AAPOS; 2007 Apr 01; 11(2):179-82. PubMed ID: 17140829
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  • 39. The human genome: chromosome 22q11 deletion syndrome.
    Morris-Rosendahl DJ, Back E.
    Am J Psychiatry; 2002 Apr 01; 159(4):527. PubMed ID: 11925287
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