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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

89 related articles for article (PubMed ID: 607767)

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

  • 22. [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]  

  • 23. [Smith-Lemli-Opitz Syndrome; endocrinologic study (author's transl)].
    Muñoz Calvo MT; Ceñal González MJ; Parra Martínez I; Hervás Olivares F; Nieto Cuartero JA; Lestache RG
    An Esp Pediatr; 1981 Nov; 15(5):498-502. PubMed ID: 7332154
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Unusual responses of muscular rigidity and hypothermia to halothane and succinylcholine; a case report of Smith-Lemli-Opitz (SLO) syndrome].
    Mizushima A; Satoyoshi M
    Masui; 1988 Sep; 37(9):1118-23. PubMed ID: 3193604
    [No Abstract]   [Full Text] [Related]  

  • 25. Diagnosis of Smith-Lemli-Opitz syndrome.
    Seedorf U; Walter M; Assmann G
    N Engl J Med; 1994 Jun; 330(23):1686-7. PubMed ID: 8177282
    [No Abstract]   [Full Text] [Related]  

  • 26. Smith-Lemli-Opitz syndrome: the changing phenotype with age.
    de Die-Smulders C; Fryns JP
    Genet Couns; 1992; 3(2):77-82. PubMed ID: 1642814
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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; 35(2-3):187-93. PubMed ID: 3612097
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Smith-Lemli-Opitz syndrome. Case report and differential diagnosis].
    Domenici R; Fiorini V; Giorgi F
    Minerva Pediatr; 1982 Sep; 34(17):709-14. PubMed ID: 6292682
    [No Abstract]   [Full Text] [Related]  

  • 29. RSH/SLO ("Smith-Lemli-Opitz") syndrome: historical, genetic, and developmental considerations.
    Opitz JM
    Am J Med Genet; 1994 May; 50(4):344-6. PubMed ID: 8209912
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Smith-Lemli-Opitz syndrome: biochemical before clinical diagnosis; early dietary management.
    Nwokoro NA; Hyde B; Mulvihill JJ
    Am J Med Genet; 1994 May; 50(4):375-6. PubMed ID: 8209919
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Smith-Lemli-Opitz syndrome. Description of 2 cases and review of the literature].
    Gemme G; Bonioli E; Ruffa G; Sbolgi P
    Minerva Pediatr; 1978 May; 30(10):805-10. PubMed ID: 672829
    [No Abstract]   [Full Text] [Related]  

  • 32. Marshall-Smith syndrome: two case reports and a review of pulmonary manifestations.
    Johnson JP; Carey JC; Glassy FJ; Paglieroni T; Lipson MH
    Pediatrics; 1983 Feb; 71(2):219-23. PubMed ID: 6823423
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Filippi syndrome: report of three additional cases.
    Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
    Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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; 26(1):45-57. PubMed ID: 3812577
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Weaver syndrome(Weaver-Smith syndrome)].
    Matsuo M
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):806-7. PubMed ID: 11529033
    [No Abstract]   [Full Text] [Related]  

  • 36. Smith-Lemli-Opitz syndrome in an inbred family.
    Nevo S; Benderly A; Levy J; Katznelson MB
    Am J Dis Child; 1972 Sep; 124(3):431-3. PubMed ID: 5056882
    [No Abstract]   [Full Text] [Related]  

  • 37. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B; Ulmer H; Müller U
    Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Intestinal aganglionosis in the Smith-Lemli-Opitz syndrome.
    Zizka J; Maresová J; Kerekes Z; Nozicka Z; Jüttnerová V; Balícek P
    Acta Paediatr Scand; 1983 Jan; 72(1):141-3. PubMed ID: 6858679
    [No Abstract]   [Full Text] [Related]  

  • 39. Two brothers with facial anomalies, microcephaly, hypoplastic genitalia, and a failure of psychomotor development.
    MacDermot KD; Winter RM
    Am J Med Genet; 1989 Jan; 32(1):60-2. PubMed ID: 2705483
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patients.
    Hershkovitz E; Shalitin S; Levy J; Leiberman E; Weinshtock A; Varsano I; Gorodischer R
    Isr J Med Sci; 1995 May; 31(5):293-7. PubMed ID: 7538982
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.