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Journal Abstract Search

178 related items for PubMed ID: 9375926

  • 1. DiGeorge anomaly and chromosome 10p deletions: one or two loci?
    Dasouki M, Jurecic V, Phillips JA, Whitlock JA, Baldini A.
    Am J Med Genet; 1997 Nov 28; 73(1):72-5. PubMed ID: 9375926
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  • 5. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA, Spikes AS, Kashork CD, Wu JM, Daw SC, Scambler PJ, Shaffer LG.
    Am J Med Genet; 2000 Apr 10; 91(4):313-7. PubMed ID: 10766989
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  • 8. Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.
    Yatsenko SA, Yatsenko AN, Szigeti K, Craigen WJ, Stankiewicz P, Cheung SW, Lupski JR.
    Clin Genet; 2004 Aug 10; 66(2):128-36. PubMed ID: 15253763
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  • 9. DiGeorge anomaly associated with 10p deletion.
    Monaco G, Pignata C, Rossi E, Mascellaro O, Cocozza S, Ciccimarra F.
    Am J Med Genet; 1991 May 01; 39(2):215-6. PubMed ID: 2063928
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  • 12. Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature.
    Dallapiccola B, Marino B, Giannotti A, Valorani G.
    Ann Genet; 1989 May 01; 32(2):92-6. PubMed ID: 2667458
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  • 15. Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications.
    Verri A, Maraschio P, Devriendt K, Uggetti C, Spadoni E, Haeusler E, Federico A.
    Ann Genet; 2004 May 01; 47(3):281-7. PubMed ID: 15337474
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  • 20. Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.
    Skrypnyk C, Goecke TO, Majewski F, Bartsch O.
    Am J Med Genet; 2002 Nov 22; 113(2):207-12. PubMed ID: 12407714
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