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Journal Abstract Search

182 related items for PubMed ID: 2330259

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  • 24. A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.
    Cobben JM, Weiss MM, van Dijk FS, De Reuver R, de Kruiff C, Pondaag W, Hennekam RC, Yntema HG.
    Eur J Med Genet; 2014; 57(11-12):636-8. PubMed ID: 25281490
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  • 32. Craniofacial disorders that have phenotypic overlap with Treacher Collins syndrome.
    Green B, Nikkhah D, Cobb AR, Dunaway DJ.
    J Plast Reconstr Aesthet Surg; 2013 Aug; 66(8):e234-5. PubMed ID: 23664577
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  • 33. The W syndrome. Studies of malformation syndromes of man XXVIII.
    Pallister PD, Herrmann J, Spranger JW, Gorlin RJ, Langer LO, Opitz JM.
    Birth Defects Orig Artic Ser; 1974 Aug; 10(7):51-60. PubMed ID: 4425540
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  • 35. [The Rieger syndrome. A clinical study. A study of 4 generations in one family with the Rieger syndrome].
    Rusu V.
    Oftalmologia; 1997 Aug; 41(3):234-7. PubMed ID: 9409970
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  • 36. [Rubinstein-Taybi-Syndrome in premature, probably identical twins].
    Holthusen W, Panteliadis C.
    Monatsschr Kinderheilkd (1902); 1971 Sep; 119(9):523-7. PubMed ID: 5097246
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  • 39. Early fatal course in three brothers with FG syndrome.
    Sorge G, Polizzi A, Ruggieri M, Smilari P, Mauceri L.
    Clin Pediatr (Phila); 1996 Jul; 35(7):365-7. PubMed ID: 8829007
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