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Journal Abstract Search

89 related items for PubMed ID: 3174148

  • 1. [Contribution to the differential diagnosis of Smith-Lemli-Opitz syndrome].
    Fehlow P.
    Padiatr Grenzgeb; 1988; 27(4):331-5. PubMed ID: 3174148
    [No Abstract] [Full Text] [Related]

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

  • 3. [Smith-Lemli-Opitz syndrome. Cardiologic considerations (author's transl)].
    Gómez de Terreros I, Cintado Bueno C, Ariza Almeida S, González Meneses A.
    An Esp Pediatr; 1975 Mar; 8(6):689-94. PubMed ID: 1211697
    [Abstract] [Full Text] [Related]

  • 4. 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
    [No Abstract] [Full Text] [Related]

  • 5. [Differential diagnosis of mentally retarded children--report of 2 cases on the Smith-Lemli-Opitz syndrome].
    Kofer J.
    Cesk Pediatr; 1976 Aug; 31(8):465-6. PubMed ID: 975364
    [No Abstract] [Full Text] [Related]

  • 6. [A typical case of Smith-Lemli-Opitz syndrome: nosologic problems and overlapping syndromes].
    Camera G.
    Pathologica; 1990 Aug; 82(1081):539-42. PubMed ID: 1964208
    [Abstract] [Full Text] [Related]

  • 7. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.
    Fischer H, Oswald HP, Duba HC, Doczy L, Simma B, Utermann G, Haas OA.
    Klin Padiatr; 1993 Aug; 205(3):162-6. PubMed ID: 8350589
    [Abstract] [Full Text] [Related]

  • 8. [Variability of the Smith-Lemli-Opitz syndrome. Report on 2 additional cases].
    Mücke J, Sandig KR, Brückner HG.
    Padiatr Grenzgeb; 1977 Aug; 16(4):221-8. PubMed ID: 600537
    [No Abstract] [Full Text] [Related]

  • 9. Floating-Harbor syndrome: case report.
    Genc G, Sarac A, Erkek Atay N, Kulali F.
    Minerva Pediatr; 2008 Apr; 60(2):249-51. PubMed ID: 18449141
    [Abstract] [Full Text] [Related]

  • 10. [Diagnosis of Edwards syndrome in newborns].
    Dunin-Wasowicz D, Krajewska-Walasek M, Rowecka-Trzebicka K, Gurkau-Malecha M, Gutkowska A, Chrzanowska K.
    Pediatr Pol; 1995 Oct; 70(10):865-74. PubMed ID: 8649934
    [Abstract] [Full Text] [Related]

  • 11. Diagnosis of Smith-Lemli-Opitz syndrome.
    McGaughran J, Donnai D, Clayton P, Mills K.
    N Engl J Med; 1994 Jun 09; 330(23):1685-6; author reply 1687. PubMed ID: 8177281
    [No Abstract] [Full Text] [Related]

  • 12. [Aniridia associated with gonadoblastoma in Smith-Lemli-Opitz syndrome (author's transl)].
    Gracia R, Nieto JA, Nistal M, Iturriaga R, Lledó G, Barrio R, Lama R.
    An Esp Pediatr; 1976 Nov 09; 9(8):19-24. PubMed ID: 1015678
    [Abstract] [Full Text] [Related]

  • 13. [Discussion contribution to the article of E. Seemanová and M. Vorísková "Smith-Lemli-Opitz syndrome in the infant" (Cs. Pediat. 29, 1974, 9 p. 504-6].
    Srsen S.
    Cesk Pediatr; 1975 Jun 09; 30(6):306-8. PubMed ID: 1157187
    [No Abstract] [Full Text] [Related]

  • 14. [Smith-Lemli-Opitz dwarfism. Report of four cases. Review of the literature].
    Cruveiller J, Msika S, Lafourcade J.
    Ann Pediatr (Paris); 1977 Dec 09; 24(12):843-51. PubMed ID: 16218266
    [No Abstract] [Full Text] [Related]

  • 15. [Smith-Lemli-Opitz syndrome in an infant].
    Seemanová E, Vorísková M.
    Cesk Pediatr; 1974 Sep 09; 29(9):504-6. PubMed ID: 4424572
    [No Abstract] [Full Text] [Related]

  • 16. Anomalies of ventricular septation and apical formation.
    Nijveldt R, Kilner PJ, Beek AM.
    Cardiol Young; 2008 Feb 09; 18(1):117-8. PubMed ID: 18031589
    [No Abstract] [Full Text] [Related]

  • 17. Two cases of severe lethal Smith-Lemli-Opitz syndrome.
    Belmont JW, Hawkins E, Hejtmancik JF, Greenberg F.
    Am J Med Genet; 1987 Jan 09; 26(1):65-7. PubMed ID: 3812579
    [No Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of Smith-Lemli-Opitz syndrome.
    McGaughran JM, Clayton PT, Mills KA, Rimmer S, Moore L, Donnai D.
    Am J Med Genet; 1995 Apr 10; 56(3):269-71. PubMed ID: 7778587
    [Abstract] [Full Text] [Related]

  • 19. Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.
    Curry CJ, Carey JC, Holland JS, Chopra D, Fineman R, Golabi M, Sherman S, Pagon RA, Allanson J, Shulman S.
    Am J Med Genet; 1987 Jan 10; 26(1):45-57. PubMed ID: 3812577
    [Abstract] [Full Text] [Related]

  • 20. Smith-Lemli-Opitz syndrome: a treatable inherited error of metabolism causing mental retardation.
    Nowaczyk MJ, Whelan DT, Heshka TW, Hill RE.
    CMAJ; 1999 Jul 27; 161(2):165-70. PubMed ID: 10439827
    [Abstract] [Full Text] [Related]

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