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Journal Abstract Search

124 related items for PubMed ID: 11242098

  • 1. Deconstructing DiGeorge syndrome.
    Schinke M, Izumo S.
    Nat Genet; 2001 Mar; 27(3):238-40. PubMed ID: 11242098
    [No Abstract] [Full Text] [Related]

  • 2. Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence.
    Mascarello JT, Bastian JF, Jones MC.
    Am J Med Genet; 1989 Jan; 32(1):112-4. PubMed ID: 2705472
    [Abstract] [Full Text] [Related]

  • 3. Genetic dissection of the DiGeorge syndrome phenotype.
    Vitelli F, Lindsay EA, Baldini A.
    Cold Spring Harb Symp Quant Biol; 2002 Jan; 67():327-32. PubMed ID: 12858556
    [No Abstract] [Full Text] [Related]

  • 4. Wrapping up DiGeorge syndrome in a T-box?
    Kim MS, Basson CT.
    Pediatr Res; 2001 Sep; 50(3):307-8. PubMed ID: 11518813
    [No Abstract] [Full Text] [Related]

  • 5. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE, Howley S, Murphy KC.
    Dev Disabil Res Rev; 2008 Sep; 14(1):26-34. PubMed ID: 18636634
    [Abstract] [Full Text] [Related]

  • 6. Interrupted aortic arch type C associated with DiGeorge syndrome in 22q11.2 deletion: first case detected in Japan.
    Fujii I, Ueno Y, Kurano R, Goto Y.
    Pediatr Int; 2005 Dec; 47(6):698-700. PubMed ID: 16354229
    [No Abstract] [Full Text] [Related]

  • 7. [22q11.2 deletion syndrome].
    Ishikawa T.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():70-3. PubMed ID: 16817353
    [No Abstract] [Full Text] [Related]

  • 8. Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
    Guris DL, Fantes J, Tara D, Druker BJ, Imamoto A.
    Nat Genet; 2001 Mar 28; 27(3):293-8. PubMed ID: 11242111
    [Abstract] [Full Text] [Related]

  • 9. Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation.
    Stoller JZ, Epstein JA.
    Hum Mol Genet; 2005 Apr 01; 14(7):885-92. PubMed ID: 15703190
    [Abstract] [Full Text] [Related]

  • 10. Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome.
    Yamagishi H, Srivastava D.
    Trends Mol Med; 2003 Sep 01; 9(9):383-9. PubMed ID: 13129704
    [Abstract] [Full Text] [Related]

  • 11. Developing models of DiGeorge syndrome.
    Epstein JA.
    Trends Genet; 2001 Oct 01; 17(10):S13-7. PubMed ID: 11585671
    [Abstract] [Full Text] [Related]

  • 12. Dissecting contiguous gene defects: TBX1.
    Baldini A.
    Curr Opin Genet Dev; 2005 Jun 01; 15(3):279-84. PubMed ID: 15917203
    [Abstract] [Full Text] [Related]

  • 13. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
    Sullivan KE.
    Immunol Allergy Clin North Am; 2008 May 01; 28(2):353-66. PubMed ID: 18424337
    [Abstract] [Full Text] [Related]

  • 14. Introduction: advances in research on velo-cardio-facial syndrome/22q11.2 deletion syndrome.
    Kates WR, Emanuel BS.
    Dev Disabil Res Rev; 2008 May 01; 14(1):1-2. PubMed ID: 18636630
    [No Abstract] [Full Text] [Related]

  • 15. 22q11 deletion syndrome: is that what they used to call . . . ?
    Umlauf MG.
    Perspect Psychiatr Care; 2008 Oct 01; 44(4):259-66. PubMed ID: 18826464
    [Abstract] [Full Text] [Related]

  • 16. 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
    [No Abstract] [Full Text] [Related]

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  • 18. [Asymptomatic extreme hypocalcemia in a 29-year old woman with CATCH 22].
    Lindstedt G, Kutti J, Swolin B, Nyström E.
    Lakartidningen; 1999 Dec 22; 96(51-52):5741-2. PubMed ID: 10643256
    [No Abstract] [Full Text] [Related]

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