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 *

132 related articles for article (PubMed ID: 3177442)

  • 1. The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS).
    Langenbeck U; Varga I; Hansmann I
    Am J Med Genet; 1988; 30(1-2):169-75. PubMed ID: 3177442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.
    Milone G; Conti L; Rizzo R; Sanfilippo S; Sammito V; Romano C
    Am J Med Genet; 1988; 30(1-2):177-83. PubMed ID: 3177443
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Institutional screening for the fragile X syndrome.
    Hagerman R; Berry R; Jackson AW; Campbell J; Smith AC; McGavran L
    Am J Dis Child; 1988 Nov; 142(11):1216-21. PubMed ID: 3177330
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dermatoglyphic indices of males with the fragile X syndrome and of the female heterozygotes.
    Simpson NE
    Am J Med Genet; 1986; 23(1-2):171-8. PubMed ID: 3953645
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study.
    Rodewald A; Froster-Iskenius U; Käb E; Langenbeck U; Schinzel A; Schmidt A; Schwinger E; Steinbach P; Veenema H; Wegner RD
    Clin Genet; 1986 Jul; 30(1):1-13. PubMed ID: 3757292
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Is there a fragile(X) negative Martin-Bell syndrome?
    Thode A; Laing S; Partington MW; Turner G
    Am J Med Genet; 1988; 30(1-2):459-71. PubMed ID: 3052069
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragile X mental retardation: prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern.
    Sanfilippo S; Ragusa RM; Musumeci S; Neri G
    Am J Med Genet; 1986; 23(1-2):589-95. PubMed ID: 3953669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dermatoglyphic findings in patients with fragile X-chromosome.
    Hirth L; Singh S; Schilling S; Müller E; Goedde HW
    Clin Genet; 1985 Feb; 27(2):118-21. PubMed ID: 3978845
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods.
    Shapiro LR; Wilmot PL; Murphy PD; Breg WR
    Am J Med Genet; 1988; 30(1-2):347-54. PubMed ID: 2902794
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fragile X expression in normal and mentally retarded subjects: effect of treatment with an antifolic agent.
    Sanfilippo S; Ragusa RM; Scillato F; Ruggeri M; Neri G
    Am J Med Genet; 1988; 30(1-2):369-76. PubMed ID: 3177459
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dermatoglyphic findings in fragile X syndrome: a causal hypothesis points to X-Y interchange.
    Loesch DZ
    Ann Hum Genet; 1986 Oct; 50(4):385-98. PubMed ID: 3442405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Crown size asymmetry in males with fra (X) or Martin-Bell syndrome.
    Peretz B; Ever-Hadani P; Casamassimo P; Eidelman E; Shellhart C; Hagerman R
    Am J Med Genet; 1988; 30(1-2):185-90. PubMed ID: 2972204
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Early manifestations of the Martin-Bell syndrome based on a series of both sexes from infancy.
    Hockey A; Crowhurst J
    Am J Med Genet; 1988; 30(1-2):61-71. PubMed ID: 3177472
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina.
    Schwartz CE; Phelan MC; Pulliam LH; Wilkes G; Vanner LV; Albiez KL; Potts WA; Rogers RC; Schroer RJ; Saul RA
    Am J Med Genet; 1988; 30(1-2):641-54. PubMed ID: 3177476
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture.
    McKinley MJ; Kearney LU; Nicolaides KH; Gosden CM; Webb TP; Fryns JP
    Am J Med Genet; 1988; 30(1-2):355-68. PubMed ID: 3177458
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The fragile X in Sicily: an epidemiological survey.
    Neri G; Sanfilippo S; Pavone L; Mollica F; Barberi I; Giuffrè L; Romano C; Mattina T; Cammarata M; Ragusa MG
    Am J Med Genet; 1988; 30(1-2):665-72. PubMed ID: 3177477
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fragile-X syndrome III: dermatoglyphic studies in males.
    Simpson NE; Newman BJ; Partington MW
    Am J Med Genet; 1984 Jan; 17(1):195-207. PubMed ID: 6711595
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.
    Mavrou A; Syrrou M; Tsenghi C; Agelakis M; Youroukos S; Metaxotou C
    Am J Med Genet; 1988 Dec; 31(4):735-9. PubMed ID: 3239562
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of a novel epileptogenic EEG pattern in the Martin-Bell syndrome.
    Musumeci SA; Ferri R; Colognola RM; Neri G; Sanfilippo S; Bergonzi P
    Am J Med Genet; 1988; 30(1-2):207-12. PubMed ID: 3177446
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
    Ventruto V; Stabile M; Gentile G; de Tollis G; Colantuoni M; Sirone P; Perone L; Lonardo F; Della Monica M; Fiore M
    Ann Genet; 1986; 29(1):59-61. PubMed ID: 3487280
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.