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Journal Abstract Search

480 related items for PubMed ID: 21167329

  • 1. Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome.
    Moortgat S, Verellen-Dumoulin C, Maystadt I, Parmentier B, Grisart B, Hennecker JL, Destree A.
    Eur J Med Genet; 2011; 54(2):177-80. PubMed ID: 21167329
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  • 3. Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus.
    Rea G, McCullough S, McNerlan S, Craig B, Morrison PJ.
    Eur J Med Genet; 2010; 53(3):162-7. PubMed ID: 20215058
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  • 7. An emerging phenotype of proximal 11q deletions.
    Melis D, Genesio R, Cozzolino M, Del Giudice E, Mormile A, Imperati F, Ronga V, Della Casa R, Nitsch L, Andria G.
    Eur J Med Genet; 2010; 53(5):340-3. PubMed ID: 20688202
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  • 8. Interstitial deletion of a proximal 3p: a clinically recognisable syndrome.
    Lalli C, Galasso C, Lo Castro A, Nardone AM, Di Paolo A, Curatolo P.
    Brain Dev; 2007 Jun; 29(5):312-6. PubMed ID: 17125947
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  • 10. Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.
    Ballarati L, Cereda A, Caselli R, Selicorni A, Recalcati MP, Maitz S, Finelli P, Larizza L, Giardino D.
    Eur J Med Genet; 2011 Jun; 54(1):55-9. PubMed ID: 20969981
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  • 11. 3p interstitial deletion: novel case report and review.
    Ţuţulan-Cunită AC, Papuc SM, Arghir A, Rötzer KM, Deshpande C, Lungeanu A, Budişteanu M.
    J Child Neurol; 2012 Aug; 27(8):1062-6. PubMed ID: 22290856
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  • 15. De novo deletion of chromosome 11q13.4-q14.3 in a boy with microcephaly, ptosis and developmental delay.
    Wincent J, Schoumans J, Anderlid BM.
    Eur J Med Genet; 2010 Aug; 53(1):50-3. PubMed ID: 19857611
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  • 18. Genotype-phenotype correlation in 13q13.3-q21.3 deletion.
    Tosca L, Brisset S, Petit FM, Metay C, Latour S, Lautier B, Lebas A, Druart L, Picone O, Mas AE, Prévot S, Tardieu M, Goossens M, Tachdjian G.
    Eur J Med Genet; 2011 Aug; 54(5):e489-94. PubMed ID: 21741501
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  • 19. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
    Shimojima K, Páez MT, Kurosawa K, Yamamoto T.
    Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
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  • 20. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
    Brenk CH, Prott EC, Trost D, Hoischen A, Walldorf C, Radlwimmer B, Wieczorek D, Propping P, Gillessen-Kaesbach G, Weber RG, Engels H.
    Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
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