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Journal Abstract Search

149 related items for PubMed ID: 1535752

  • 1. Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington disease.
    Ikonen E, Salo A, Somer M, Somer H, Pääkkönen L, Peltonen L.
    Am J Med Genet; 1992 Jul 01; 43(4):753-8. PubMed ID: 1535752
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  • 2. On the deletion 4p16 Wolf-Hirschhorn syndrome.
    Rivas F, Hernandez A, Nazara Z, Fragoso R, Olivares N, Rolon A, Cantu JM.
    Ann Genet; 1979 Jul 01; 22(4):228-31. PubMed ID: 317787
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  • 3. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H.
    Ann Genet; 1989 Jul 01; 32(1):59-61. PubMed ID: 2751251
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  • 4. Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother.
    Fryns JP, Smeets E, Devriendt K, Petit P.
    Ann Genet; 1998 Jul 01; 41(2):73-6. PubMed ID: 9706336
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  • 5. "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.
    Zollino M, Wright TJ, Di Stefano C, Tosolini A, Battaglia A, Altherr MR, Neri G.
    Am J Med Genet; 1999 Feb 19; 82(5):371-5. PubMed ID: 10069706
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  • 12. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M, Murdolo M, Marangi G, Pecile V, Galasso C, Mazzanti L, Neri G.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):257-69. PubMed ID: 18932124
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  • 13. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun 15; 25(6):451-5. PubMed ID: 15966060
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  • 14. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
    Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF.
    Am J Med Genet; 1997 Sep 05; 71(4):453-7. PubMed ID: 9286454
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  • 19. A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.
    Goodship J, Curtis A, Cross I, Brown J, Emslie J, Wolstenholme J, Bhattacharya S, Burn J.
    J Med Genet; 1992 Jul 05; 29(7):451-4. PubMed ID: 1640422
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