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Journal Abstract Search

233 related items for PubMed ID: 8182713

  • 1. Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.
    Estabrooks LL, Lamb AN, Aylsworth AS, Callanan NP, Rao KW.
    J Med Genet; 1994 Feb; 31(2):103-7. PubMed ID: 8182713
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  • 2. Clinical, cytogenetic and molecular investigations in three patients with Wolf-Hirschhorn syndrome.
    Thies U, Back E, Wolff G, Schroeder-Kurth T, Hager HD, Schröder K.
    Clin Genet; 1992 Oct; 42(4):201-5. PubMed ID: 1424245
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  • 3. Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.
    Kant SG, Van Haeringen A, Bakker E, Stec I, Donnai D, Mollevanger P, Beverstock GC, Lindeman-Kusse MC, Van Ommen GJ.
    J Med Genet; 1997 Jul; 34(7):569-72. PubMed ID: 9222965
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  • 4. Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.
    Anvret M, Nordenskjöld M, Stolpe L, Johansson L, Bröndum-Nielsen K.
    Hum Genet; 1991 Mar; 86(5):481-3. PubMed ID: 2016087
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  • 5. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
    Bi W, Cheung SW, Breman AM, Bacino CA.
    Am J Med Genet A; 2016 Oct; 170(10):2540-50. PubMed ID: 27287194
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  • 8. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
    Finzi S, Pinto CF, Wiggs JL.
    Ophthalmic Genet; 2001 Mar; 22(1):35-41. PubMed ID: 11262648
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  • 9. Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.
    Zollino M, Lecce R, Murdolo M, Orteschi D, Marangi G, Selicorni A, Midro A, Sorge G, Zampino G, Memo L, Battaglia D, Petersen M, Pandelia E, Gyftodimou Y, Faravelli F, Tenconi R, Garavelli L, Mazzanti L, Fischetto R, Cavalli P, Savasta S, Rodriguez L, Neri G.
    Hum Genet; 2007 Dec; 122(5):423-30. PubMed ID: 17676343
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  • 11. Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome.
    Dallapiccola B, Mandich P, Bellone E, Selicorni A, Mokin V, Ajmar F, Novelli G.
    Am J Med Genet; 1993 Nov 01; 47(6):921-4. PubMed ID: 7904122
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  • 12. Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.
    Martsolf JT, Chase TR, Jalal SM, Wasdahl WA.
    Clin Genet; 1987 Jun 01; 31(6):366-9. PubMed ID: 3621637
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  • 13. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.
    Zollino M, Di Stefano C, Zampino G, Mastroiacovo P, Wright TJ, Sorge G, Selicorni A, Tenconi R, Zappalà A, Battaglia A, Di Rocco M, Palka G, Pallotta R, Altherr MR, Neri G.
    Am J Med Genet; 2000 Sep 18; 94(3):254-61. PubMed ID: 10995514
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  • 14. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
    Estabrooks LL, Rao KW, Korf B.
    Am J Med Genet; 1993 Jan 01; 45(1):97-100. PubMed ID: 8418669
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  • 15. Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.
    Quarrell OW, Snell RG, Curtis MA, Roberts SH, Harper PS, Shaw DJ.
    J Med Genet; 1991 Apr 01; 28(4):256-9. PubMed ID: 1856831
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  • 16. Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.
    McKeown C, Read AP, Dodge A, Stecko O, Mercer A, Harris R.
    J Med Genet; 1987 Jul 01; 24(7):410-2. PubMed ID: 3612716
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  • 17. Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.
    Tupler R, Bortotto L, Bühler EM, Alkan M, Malik NJ, Bösch-Al Jadooa N, Memo L, Maraschio P.
    J Med Genet; 1992 Jan 01; 29(1):53-5. PubMed ID: 1552546
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  • 20. A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome.
    Zollino M, Lecce R, Selicorni A, Murdolo M, Mancuso I, Marangi G, Zampino G, Garavelli L, Ferrarini A, Rocchi M, Opitz JM, Neri G.
    Eur J Hum Genet; 2004 Oct 01; 12(10):797-804. PubMed ID: 15241479
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