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Journal Abstract Search

230 related items for PubMed ID: 4386913

  • 1. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.
    Park SC, Needles CF, Dimich I, Sussman L.
    J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913
    [No Abstract] [Full Text] [Related]

  • 2. Craniofacial manifestations of Smith-Lemli-Opitz syndrome: case report.
    Antoniades K, Peonidis A, Pehlivanidis C, Kavadia S, Panagiotidis P.
    Int J Oral Maxillofac Surg; 1994 Dec; 23(6 Pt 1):363-5. PubMed ID: 7699276
    [Abstract] [Full Text] [Related]

  • 3. Associated acral and renal malformations: a new syndrome?
    Curran AS, Curran JP.
    Pediatrics; 1972 May; 49(5):716-25. PubMed ID: 4402497
    [No Abstract] [Full Text] [Related]

  • 4. Picture of the month. Smith-Lemli-Opitz syndrome.
    Sood S, Giacoia GP, Tunnessen WW.
    Arch Pediatr Adolesc Med; 1994 Nov; 148(11):1189-90. PubMed ID: 7921121
    [No Abstract] [Full Text] [Related]

  • 5. Smith-Lemli-Opitz syndrome: review and report of two affected siblings.
    Johnson VP.
    Z Kinderheilkd; 1975 Nov; 119(4):221-34. PubMed ID: 166525
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  • 6. The Smith-Lemli-Opitz syndrome.
    Judge CG, Chakanovskis JE, Sutherland GR.
    Med J Aust; 1971 Jul 17; 2(3):145-7. PubMed ID: 5096180
    [No Abstract] [Full Text] [Related]

  • 7. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 17; 14(2):91-2. PubMed ID: 8469651
    [No Abstract] [Full Text] [Related]

  • 8. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
    Dallaire L.
    J Med Genet; 1969 Jun 17; 6(2):113-20. PubMed ID: 4389828
    [No Abstract] [Full Text] [Related]

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  • 10. [Two malformative syndromes possibly unifiable: Ullrich-Feichtiger and Smith-Lemli-Opitz syndromes. Case report].
    Lendvai D, Castello MA, Ballati G.
    Minerva Pediatr; 1969 Jan 14; 21(2):56-61. PubMed ID: 4388355
    [No Abstract] [Full Text] [Related]

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  • 14. [Ullrich-Feichtiger's syndrome].
    Kunze J.
    Arch Kinderheilkd; 1969 Jul 14; 179(2):182-6. PubMed ID: 5802844
    [No Abstract] [Full Text] [Related]

  • 15. An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosis.
    Pfeiffer RA, Tietze U, Welte W.
    Eur J Pediatr; 1987 Jan 14; 146(1):74-5. PubMed ID: 3034618
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  • 17. [Infantile spasms in monozygotic twins with Smith-Lemli-Opitz syndrome type I].
    Itokazu N, Ohba K, Sonoda T, Ohdo S.
    No To Hattatsu; 1992 Sep 14; 24(5):485-90. PubMed ID: 1389333
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  • 18. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D, Farriaux JP.
    J Genet Hum; 1971 Dec 14; 19(4):299-316. PubMed ID: 5152131
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