BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 10405444)

  • 1. Clinical and behavioral characteristics in FG syndrome.
    Graham JM; Superneau D; Rogers RC; Corning K; Schwartz CE; Dykens EM
    Am J Med Genet; 1999 Aug; 85(5):470-5. PubMed ID: 10405444
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FG syndrome: report of three new families with linkage to Xq12-q22.1.
    Graham JM; Tackels D; Dibbern K; Superneau D; Rogers C; Corning K; Schwartz CE
    Am J Med Genet; 1998 Nov; 80(2):145-56. PubMed ID: 9805132
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
    Zwamborn-Hanssen AM; Schrander-Stumpel CT; Smeets E; Decock P; Fryns JP
    Genet Couns; 1995; 6(4):313-9. PubMed ID: 8775418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 gene.
    Graham JM; Visootsak J; Dykens E; Huddleston L; Clark RD; Jones KL; Moeschler JB; Opitz JM; Morford J; Simensen R; Rogers RC; Schwartz CE; Friez MJ; Stevenson RE
    Am J Med Genet A; 2008 Dec; 146A(23):3011-7. PubMed ID: 18973276
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3].
    Dessay S; Moizard MP; Gilardi JL; Opitz JM; Middleton-Price H; Pembrey M; Moraine C; Briault S
    Am J Med Genet; 2002 Sep; 112(1):6-11. PubMed ID: 12239712
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Refining behavioral phenotypes: personality-motivation in Williams and Prader-Willi syndromes.
    Dykens EM; Rosner BA
    Am J Ment Retard; 1999 Mar; 104(2):158-69. PubMed ID: 10207579
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.
    Lyons MJ; Graham JM; Neri G; Hunter AG; Clark RD; Rogers RC; Moscarda M; Boccuto L; Simensen R; Dodd J; Robertson S; DuPont BR; Friez MJ; Schwartz CE; Stevenson RE
    J Med Genet; 2009 Jan; 46(1):9-13. PubMed ID: 18805826
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6.
    Visootsak J; Rosner B; Dykens E; Schwartz C; Hahn K; White SM; Szeftel R; Graham JM
    J Pediatr; 2004 Dec; 145(6):819-25. PubMed ID: 15580208
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The FG syndrome: further characterization, report of a third family, and of a sporadic case.
    Riccardi VM; Hässler E; Lubinsky MS
    Am J Med Genet; 1977; 1(1):47-58. PubMed ID: 565138
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The neurofaciodigitorenal (NFDR) syndrome.
    Freire-Maia N; Pinheiro M; Opitz JM
    Am J Med Genet; 1982 Mar; 11(3):329-36. PubMed ID: 7081297
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Behavioral features of CHARGE syndrome (Hall-Hittner syndrome) comparison with Down syndrome, Prader-Willi syndrome, and Williams syndrome.
    Graham JM; Rosner B; Dykens E; Visootsak J
    Am J Med Genet A; 2005 Mar; 133A(3):240-7. PubMed ID: 15637708
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [FG syndrome in 2 half brothers].
    Wieg C; Meinecke P
    Monatsschr Kinderheilkd; 1991 Oct; 139(10):687-9. PubMed ID: 1961207
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A gene for FG syndrome maps in the Xq12-q21.31 region.
    Briault S; Hill R; Shrimpton A; Zhu D; Till M; Ronce N; Margaritte-Jeannin P; Baraitser M; Middleton-Price H; Malcolm S; Thompson E; Hoo J; Wilson G; Romano C; Guichet A; Pembrey M; Fontes M; Poustka A; Moraine C
    Am J Med Genet; 1997 Nov; 73(1):87-90. PubMed ID: 9375929
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome).
    Graham JM; Clark RD; Moeschler JB; Rogers RC
    Am J Med Genet C Semin Med Genet; 2010 Nov; 154C(4):477-85. PubMed ID: 20981778
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation.
    Dykens EM; Kasari C
    Am J Ment Retard; 1997 Nov; 102(3):228-37. PubMed ID: 9394132
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Japanese kindred with FG syndrome.
    Kato R; Niikawa N; Nagai T; Fukushima Y
    Am J Med Genet; 1994 Aug; 52(2):242-3. PubMed ID: 7802020
    [No Abstract]   [Full Text] [Related]  

  • 17. Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome.
    van Lieshout CF; De Meyer RE; Curfs LM; Fryns JP
    J Child Psychol Psychiatry; 1998 Jul; 39(5):699-710. PubMed ID: 9690933
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE; Kimonis VE; Morales A
    Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The FG syndrome: report of a large Italian series.
    Battaglia A; Chines C; Carey JC
    Am J Med Genet A; 2006 Oct; 140(19):2075-9. PubMed ID: 16691600
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genitourinary anomalies of pediatric FG syndrome.
    Smith JF; Wayment RO; Cartwright PC; Snow BW; Opitz JM
    J Urol; 2007 Aug; 178(2):656-9. PubMed ID: 17574621
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.