473 related articles for article (PubMed ID: 11173318)
1. Borjeson-Forssman-Lehmann syndrome and dilated cardiomyopathy: a previously unreported association.
Kaplinsky E; Perandones C; Galiana MG; Fideleff H; Favaloro RR; Carlos V; Perrone SV
Can J Cardiol; 2001 Jan; 17(1):80-3. PubMed ID: 11173318
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Microencephalic nanism, severe retardation, hypertonia, obesity, and hypogonadism in two brothers: a new syndrome?].
Delozier-Blanchet CD; Haenggeli CA; Engel E
J Genet Hum; 1989 Dec; 37(4-5):353-65. PubMed ID: 2635712
[TBL] [Abstract][Full Text] [Related]
4. Dermatoglyphics in Börjeson-Forssman-Lehmann syndrome.
Flannery DB; Piussan C; Wright LE
Am J Med Genet; 1985 Jun; 21(2):401-4. PubMed ID: 4014320
[No Abstract] [Full Text] [Related]
5. Börjeson-Forssman-Lehmann syndrome in a woman with skewed X-chromosome inactivation.
Kubota T; Oga S; Ohashi H; Iwamoto Y; Fukushima Y
Am J Med Genet; 1999 Nov; 87(3):258-61. PubMed ID: 10564881
[TBL] [Abstract][Full Text] [Related]
6. New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.
Wilson M; Mulley J; Gedeon A; Robinson H; Turner G
Am J Med Genet; 1991 Sep; 40(4):406-13. PubMed ID: 1746601
[TBL] [Abstract][Full Text] [Related]
7. The Borjeson-Forssman-Lehmann syndrome. A family study.
Dereymaeker AM; Fryns JP; Hoefnagels M; Heremans G; Marien J; van den Berghe H
Clin Genet; 1986 Apr; 29(4):317-20. PubMed ID: 3720009
[TBL] [Abstract][Full Text] [Related]
8. [Börjeson-Forssman-Lehmann syndrome].
Kubota T
Ryoikibetsu Shokogun Shirizu; 2001; (33):284-5. PubMed ID: 11462441
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Börjeson-Forssman-Lehmann syndrome localization.
Mathews KD; Buetow K; Turner G; Mulley J
Am J Med Genet; 1989 Dec; 34(4):475. PubMed ID: 2491427
[No Abstract] [Full Text] [Related]
13. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
Lin AE
Am J Med Genet; 1993 Jun; 46(5):606-7. PubMed ID: 8322829
[No Abstract] [Full Text] [Related]
14. 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]
15. [Börjeson-Forssman-Lehmann syndrome].
Kubota T
Nihon Rinsho; 2006 Sep; Suppl 3():410-2. PubMed ID: 17022575
[No Abstract] [Full Text] [Related]
16. Borjeson-Forssman-Lehmann syndrome in a girl.
Matsuo K; Murano I; Kajii T
Jinrui Idengaku Zasshi; 1984 Jun; 29(2):121-6. PubMed ID: 6439922
[No Abstract] [Full Text] [Related]
17. 1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family.
Lower KM; Solders G; Bondeson ML; Nelson J; Brun A; Crawford J; Malm G; Börjeson M; Turner G; Partington M; Gécz J
Eur J Hum Genet; 2004 Oct; 12(10):787-9. PubMed ID: 15241480
[No Abstract] [Full Text] [Related]
18. 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]
19. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
Gurrieri F; Cappa M; Neri G
Am J Med Genet; 1992 Sep; 44(2):136-7. PubMed ID: 1456280
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
