These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


105 related items for PubMed ID: 8533850

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villi.
    Linck LM, Hayflick SJ, Lin DS, Battaile KP, Ginat S, Burlingame T, Gibson KM, Honda M, Honda A, Salen G, Tint GS, Connor WE, Steiner RD.
    Prenat Diagn; 2000 Mar; 20(3):238-40. PubMed ID: 10719329
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of holoprosencephaly associated with Smith-Lemli-Opitz syndrome (SLOS) in a 46,XX fetus.
    Travessa A, Dias P, Rocha P, Sousa AB.
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):541-544. PubMed ID: 28805615
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. First-trimester diagnosis of Smith-Lemli-Opitz syndrome.
    Sharp P, Haan E, Fletcher JM, Khong TY, Carey WF.
    Prenat Diagn; 1997 Apr; 17(4):355-61. PubMed ID: 9160388
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Trends in prenatal diagnosis of non-specific multiple malformations disorders with reference to the own experience and research study on Smith-Lemli-Opitz syndrome.
    Jezela-Stanek A, Małunowicz E, Anna S, Kucharczyk M, Goryluk-Kozakiewicz B, Sodowska H, Krajewska-Walasek M.
    Ginekol Pol; 2015 Aug; 86(8):598-602. PubMed ID: 26492708
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Defective conversion of 7-dehydrocholesterol to cholesterol in cultured skin fibroblasts from Smith-Lemli-Opitz syndrome homozygotes.
    Honda A, Tint GS, Salen G, Batta AK, Chen TS, Shefer S.
    J Lipid Res; 1995 Jul; 36(7):1595-601. PubMed ID: 7595082
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of Smith-Lemli-Opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid.
    Dallaire L, Mitchell G, Giguère R, Lefebvre F, Melançon SB, Lambert M.
    Prenat Diagn; 1995 Sep; 15(9):855-8. PubMed ID: 8559757
    [Abstract] [Full Text] [Related]

  • 15. Trisomy 18: first-trimester nuchal translucency with pathological correlation.
    Jackson S, Porter H, Vyas S.
    Ultrasound Obstet Gynecol; 1995 Jan; 5(1):55-6. PubMed ID: 7850592
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome.
    Nowaczyk MJ, Heshka T, Kratz LE, Kelley RE.
    Am J Med Genet; 2000 Dec 11; 95(4):396-8. PubMed ID: 11186897
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Abnormal first-trimester fetal nuchal translucency and Cornelia De Lange syndrome.
    Huang WH, Porto M.
    Obstet Gynecol; 2002 May 11; 99(5 Pt 2):956-8. PubMed ID: 11975974
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 6.