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Journal Abstract Search

307 related items for PubMed ID: 17022067

  • 1. Microarray-based comparative genomic hybridization analysis of Wolf-Hirschhorn syndrome in a fetus with deletion of 4p15.3 to 4pter.
    Chao A, Lee YS, Chao AS, Wang TH, Chang SD.
    Birth Defects Res A Clin Mol Teratol; 2006 Oct; 76(10):739-43. PubMed ID: 17022067
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  • 2. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G, Mobili L, Braguglia A, Santoro F, Bagolan P.
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
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  • 3. 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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  • 4. Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
    South ST, Whitby H, Battaglia A, Carey JC, Brothman AR.
    Eur J Hum Genet; 2008 Jan 15; 16(1):45-52. PubMed ID: 17726485
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  • 5. 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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  • 8. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.
    Battaglia A, Filippi T, Carey JC.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):246-51. PubMed ID: 18932224
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  • 9. Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.
    Laleye A, Alao MJ, Adjagba M, Hans C, Delneste D, Gnamey DK, Ayivi B, Darboux RB.
    Genet Couns; 2006 Nov 15; 17(1):35-40. PubMed ID: 16719275
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  • 11. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G.
    Eur J Hum Genet; 2000 Jul 15; 8(7):519-26. PubMed ID: 10909852
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  • 12. 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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  • 13. 4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotype.
    Stevenson DA, Carey JC, Cowley BC, Bayrak-Toydemir P, Mao R, Brothman AR.
    J Pediatr; 2004 Dec 01; 145(6):840-2. PubMed ID: 15580214
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  • 14. Wolf-Hirschhorn (4P-) syndrome in adults.
    Marcelis C, Schrander-Stumpel C, Engelen J, Schoonbrood-Lenssen A, Willemse A, Beemer F, Sigaudy S, Missirian C, Philip N, Fryns JP.
    Genet Couns; 2001 Dec 01; 12(1):35-48. PubMed ID: 11332977
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  • 15. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec 01; 50(4):506-11. PubMed ID: 22212326
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  • 16. [Wolf-Hirschhorn syndrome].
    Heljić S, Catibusić F, Dozić M, Mackić M.
    Med Arh; 2004 Dec 01; 58(5):318-20. PubMed ID: 15628261
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  • 17. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
    Gawlik-Kuklinska K, Wierzba J, Wozniak A, Iliszko M, Debiec-Rychter M, Dubaniewicz-Wybieralska M, Limon J.
    Eur J Med Genet; 2008 Dec 01; 51(2):165-71. PubMed ID: 18243084
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  • 18. 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. Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome.
    Altherr MR, Gusella JF, Wasmuth JJ, Kummer MA, McKercher SW, Johnson VP.
    Am J Med Genet; 1992 Nov 01; 44(4):449-54. PubMed ID: 1442886
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