181 related articles for article (PubMed ID: 15580208)
1. 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]
2. Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome.
Lower KM; Turner G; Kerr BA; Mathews KD; Shaw MA; Gedeon AK; Schelley S; Hoyme HE; White SM; Delatycki MB; Lampe AK; Clayton-Smith J; Stewart H; van Ravenswaay CM; de Vries BB; Cox B; Grompe M; Ross S; Thomas P; Mulley JC; Gécz J
Nat Genet; 2002 Dec; 32(4):661-5. PubMed ID: 12415272
[TBL] [Abstract][Full Text] [Related]
3. Börjeson-Forssman-Lehmann Syndrome due to a novel plant homeodomain zinc finger mutation in the PHF6 gene.
Mangelsdorf M; Chevrier E; Mustonen A; Picketts DJ
J Child Neurol; 2009 May; 24(5):610-4. PubMed ID: 19264739
[TBL] [Abstract][Full Text] [Related]
4. Börjeson-Forssman-Lehmann syndrome: further delineation in five cases.
Ardinger HH; Hanson JW; Zellweger HU
Am J Med Genet; 1984 Dec; 19(4):653-64. PubMed ID: 6517094
[TBL] [Abstract][Full Text] [Related]
5. Behavioural phenotype in Börjeson-Forssman-Lehmann syndrome.
de Winter CF; van Dijk F; Stolker JJ; Hennekam RC
J Intellect Disabil Res; 2009 Apr; 53(4):319-28. PubMed ID: 19187102
[TBL] [Abstract][Full Text] [Related]
6. Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.
Voss AK; Gamble R; Collin C; Shoubridge C; Corbett M; Gécz J; Thomas T
Gene Expr Patterns; 2007 Oct; 7(8):858-71. PubMed ID: 17698420
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The Börjeson-Forssman-Lehman syndrome (BFLS, MIM #301900).
Gécz J; Turner G; Nelson J; Partington M
Eur J Hum Genet; 2006 Dec; 14(12):1233-7. PubMed ID: 16912705
[TBL] [Abstract][Full Text] [Related]
9. Linkage localization of Börjeson-Forssman-Lehmann syndrome.
Mathews KD; Ardinger HH; Nishimura DY; Buetow KH; Murray JC; Bartley JA
Am J Med Genet; 1989 Dec; 34(4):470-4. PubMed ID: 2624254
[TBL] [Abstract][Full Text] [Related]
10. Mutation screening in Borjeson-Forssman-Lehmann syndrome: identification of a novel de novo PHF6 mutation in a female patient.
Crawford J; Lower KM; Hennekam RC; Van Esch H; Mégarbané A; Lynch SA; Turner G; Gécz J
J Med Genet; 2006 Mar; 43(3):238-43. PubMed ID: 15994862
[TBL] [Abstract][Full Text] [Related]
11. Adaptive and maladaptive behavior in Prader-Willi syndrome.
Dykens EM; Hodapp RM; Walsh K; Nash LJ
J Am Acad Child Adolesc Psychiatry; 1992 Nov; 31(6):1131-6. PubMed ID: 1429417
[TBL] [Abstract][Full Text] [Related]
12. Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.
Turner G; Gedeon A; Mulley J; Sutherland G; Rae J; Power K; Arthur I
Am J Med Genet; 1989 Dec; 34(4):463-9. PubMed ID: 2624253
[TBL] [Abstract][Full Text] [Related]
13. Further clinical delineation of the Börjeson-Forssman-Lehmann syndrome in patients with PHF6 mutations.
Carter MT; Picketts DJ; Hunter AG; Graham GE
Am J Med Genet A; 2009 Feb; 149A(2):246-50. PubMed ID: 19161141
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome?
Verloes A; Gillerot Y; Delfortrie J; Zeevaert-Arnold MT; Collard R; Koulischer L; Fryns JP
Genet Couns; 1990; 1(3-4):219-25. PubMed ID: 2098045
[TBL] [Abstract][Full Text] [Related]
16. The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations.
Turner G; Lower KM; White SM; Delatycki M; Lampe AK; Wright M; Smith JC; Kerr B; Schelley S; Hoyme HE; De Vries BB; Kleefstra T; Grompe M; Cox B; Gecz J; Partington M
Clin Genet; 2004 Mar; 65(3):226-32. PubMed ID: 14756673
[TBL] [Abstract][Full Text] [Related]
17. Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.
Zweier C; Rittinger O; Bader I; Berland S; Cole T; Degenhardt F; Di Donato N; Graul-Neumann L; Hoyer J; Lynch SA; Vlasak I; Wieczorek D
Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):290-301. PubMed ID: 25099957
[TBL] [Abstract][Full Text] [Related]
18. Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome.
Gedeon AK; Kozman HM; Robinson H; Pilia G; Schlessinger D; Turner G; Mulley JC
Am J Med Genet; 1996 Jul; 64(1):63-8. PubMed ID: 8826450
[TBL] [Abstract][Full Text] [Related]
19. The Börjeson-Forssman-Lehmann syndrome.
Robinson LK; Jones KL; Culler F; Nyhan WL; Sakati N; Jones KL
Am J Med Genet; 1983 Jul; 15(3):457-68. PubMed ID: 6683929
[TBL] [Abstract][Full Text] [Related]
20. A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype.
Zweier C; Kraus C; Brueton L; Cole T; Degenhardt F; Engels H; Gillessen-Kaesbach G; Graul-Neumann L; Horn D; Hoyer J; Just W; Rauch A; Reis A; Wollnik B; Zeschnigk M; Lüdecke HJ; Wieczorek D
J Med Genet; 2013 Dec; 50(12):838-47. PubMed ID: 24092917
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
