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Journal Abstract Search

83 related items for PubMed ID: 3564150

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  • 4. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
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  • 7. [An autopsy case of Smith-Lemli-Opitz syndrome].
    Nagao M, Iwadate K, Zhang WD, Takahashi H, Yamada Y, Suzuki H, Takatori T.
    Nihon Hoigaku Zasshi; 1994 Aug; 48(4):274-8. PubMed ID: 7967168
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  • 8. Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome.
    Witsch-Baumgartner M, Gruber M, Kraft HG, Rossi M, Clayton P, Giros M, Haas D, Kelley RI, Krajewska-Walasek M, Utermann G.
    J Med Genet; 2004 Aug; 41(8):577-84. PubMed ID: 15286151
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  • 9. Brief clinical report: familial neonatally lethal syndrome of hypoplastic left heart, absent pulmonary lobation, polydactyly, and talipes, probably Smith-Lemli-Opitz (RSH) syndrome.
    Kohler HG.
    Am J Med Genet; 1983 Mar; 14(3):423-8. PubMed ID: 6859093
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  • 10. Editorial comment: variability in the Smith-Lemli-Opitz syndrome: overlap with the Meckel syndrome.
    Lowry RB.
    Am J Med Genet; 1983 Mar; 14(3):429-33. PubMed ID: 6859094
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  • 11. Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?
    Alkuraya FS, Picker J, Irons MB, Kimonis VE.
    Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):569-71. PubMed ID: 15965973
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  • 12. Cardiovascular malformations in Smith-Lemli-Opitz syndrome.
    Lin AE, Ardinger HH, Ardinger RH, Cunniff C, Kelley RI.
    Am J Med Genet; 1997 Jan 31; 68(3):270-8. PubMed ID: 9024558
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  • 14. [A typical case of Smith-Lemli-Opitz syndrome: nosologic problems and overlapping syndromes].
    Camera G.
    Pathologica; 1990 Jan 31; 82(1081):539-42. PubMed ID: 1964208
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  • 17. [An unrecognized etiology of sexual ambiguity: Smith-Lemli-Opitz syndrome or a new entity?].
    Le Merrer M, Briard ML, Chauvet ML.
    J Genet Hum; 1987 May 31; 35(2-3):187-93. PubMed ID: 3612097
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  • 18. Phenotypic diversity in the Smith-Lemli-Opitz syndrome.
    Seller MJ, Flinter FA, Docherty Z, Fagg N, Newbould M.
    Clin Dysmorphol; 1997 Jan 31; 6(1):69-73. PubMed ID: 9018421
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  • 19. Familial broad terminal phalanges with one individual showing additional anomalies.
    Pavone L, Sorge G, Pavone V, Rizzo R, Ruggieri M, Polizzi A, Opitz JM.
    Am J Med Genet; 1997 Aug 22; 71(3):271-4. PubMed ID: 9268094
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