154 related articles for article (PubMed ID: 11415514)
1. Ring-X chromosomes: their cognitive and behavioural phenotype.
Kuntsi J; Skuse D; Elgar K; Morris E; Turner C
Ann Hum Genet; 2000 Jul; 64(Pt 4):295-305. PubMed ID: 11415514
[TBL] [Abstract][Full Text] [Related]
2. A clinical, cytogenetic and molecular study of 47 females with r(X) chromosomes.
Dennis N; Coppin B; Turner C; Skuse D; Jacobs P
Ann Hum Genet; 2000 Jul; 64(Pt 4):277-93. PubMed ID: 11415513
[TBL] [Abstract][Full Text] [Related]
3. Molecular characterization of tiny ring X chromosomes from females with functional X chromosome disomy and lack of cis X inactivation.
Jani MM; Torchia BS; Pai GS; Migeon BR
Genomics; 1995 May; 27(1):182-8. PubMed ID: 7665167
[TBL] [Abstract][Full Text] [Related]
4. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
[TBL] [Abstract][Full Text] [Related]
5. Severe phenotypes associated with inactive ring X chromosomes.
Migeon BR; Ausems M; Giltay J; Hasley-Royster C; Kazi E; Lydon TJ; Engelen JJ; Raymond GV
Am J Med Genet; 2000 Jul; 93(1):52-7. PubMed ID: 10861682
[TBL] [Abstract][Full Text] [Related]
6. 45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome.
Grompe M; Rao N; Elder FF; Caskey CT; Greenberg F
Am J Med Genet; 1992 Jan; 42(1):39-43. PubMed ID: 1339199
[TBL] [Abstract][Full Text] [Related]
7. Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
Leppig KA; Disteche CM
Semin Reprod Med; 2001 Jun; 19(2):147-57. PubMed ID: 11480912
[TBL] [Abstract][Full Text] [Related]
8. An atypical Turner syndrome patient with ring X chromosome mosaicism.
Cantú ES; Jacobs DF; Pai GS
Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
[TBL] [Abstract][Full Text] [Related]
9. X-inactivation pattern in an Ullrich-Turner syndrome patient with a small ring X and normal intelligence.
Zenger-Hain JL; Wiktor A; Goldman J; Van Dyke DL; Weiss L
Am J Med Genet; 1993 Sep; 47(4):490-3. PubMed ID: 8256812
[TBL] [Abstract][Full Text] [Related]
10. Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay.
Tomkins DJ; McDonald HL; Farrell SA; Brown CJ
Eur J Hum Genet; 2002 Jan; 10(1):44-51. PubMed ID: 11896455
[TBL] [Abstract][Full Text] [Related]
11. Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis.
Bouayed Abdelmoula N; Portnoï MF; Amouri A; Arladan A; Chakroun M; Saad A; Hchicha M; Turki H; Rebai T
Ann Genet; 2004; 47(3):305-13. PubMed ID: 15337477
[TBL] [Abstract][Full Text] [Related]
12. Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation.
Van Dyke DL; Wiktor A; Palmer CG; Miller DA; Witt M; Babu VR; Worsham MJ; Roberson JR; Weiss L
Am J Med Genet; 1992 Aug; 43(6):996-1005. PubMed ID: 1415351
[TBL] [Abstract][Full Text] [Related]
13. The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females.
Kubota T; Wakui K; Nakamura T; Ohashi H; Watanabe Y; Yoshino M; Kida T; Okamoto N; Matsumura M; Muroya K; Ogata T; Goto Y; Fukushima Y
Cytogenet Genome Res; 2002; 99(1-4):276-84. PubMed ID: 12900575
[TBL] [Abstract][Full Text] [Related]
14. Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotype.
Turner C; Dennis NR; Skuse DH; Jacobs PA
Hum Genet; 2000 Jan; 106(1):93-100. PubMed ID: 10982188
[TBL] [Abstract][Full Text] [Related]
15. Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes.
Yorifuji T; Muroi J; Kawai M; Uematsu A; Sasaki H; Momoi T; Kaji M; Yamanaka C; Furusho K
J Med Genet; 1998 Jul; 35(7):539-44. PubMed ID: 9678697
[TBL] [Abstract][Full Text] [Related]
16. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
17. High incidence of mental retardation in Turner syndrome patients with ring chromosome X formation.
Fryns JP; Kleczkowska A; Van Den Berghe H
Genet Couns; 1990; 1(2):161-5. PubMed ID: 2080999
[TBL] [Abstract][Full Text] [Related]
18. Molecular-neurobehavioral associations in females with the fragile X full mutation.
Abrams MT; Reiss AL; Freund LS; Baumgardner TL; Chase GA; Denckla MB
Am J Med Genet; 1994 Jul; 51(4):317-27. PubMed ID: 7942994
[TBL] [Abstract][Full Text] [Related]
19. The severe phenotype of females with tiny ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation.
Migeon BR; Luo S; Jani M; Jeppesen P
Am J Hum Genet; 1994 Sep; 55(3):497-504. PubMed ID: 8079992
[TBL] [Abstract][Full Text] [Related]
20. Three patients with ring (X) chromosomes and a severe phenotype.
Dennis NR; Collins AL; Crolla JA; Cockwell AE; Fisher AM; Jacobs PA
J Med Genet; 1993 Jun; 30(6):482-6. PubMed ID: 8326492
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
