BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 1415351)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
    Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT
    Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446
    [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. 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]  

  • 10. 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]  

  • 11. 45X/46X,r(X) with syndactyly and severe mental retardation.
    Kushnick T; Irons TG; Wiley JE; Gettig EA; Rao KW; Bowyer S
    Am J Med Genet; 1987 Nov; 28(3):567-74. PubMed ID: 2827478
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
    Lin CC; Meyne J; Sasi R; Bowen P; Unger T; Tainaka T; Hadro TA; Hoo JJ
    Am J Med Genet; 1990 Sep; 37(1):71-8. PubMed ID: 2240047
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Novel ring chromosome composed of X- and Y-derived material in a girl with manifestations of Ullrich-Turner syndrome.
    Grass FS; Brown CA; Backeljauw PF; Lucas A; Brasington C; Gazak JM; Nakano S; Ostrowski RS; Spence JE
    Am J Med Genet; 2000 Aug; 93(5):343-8. PubMed ID: 10951455
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. PCR-based study of the presence of Y-chromosome sequences in patients with Ullrich-Turner syndrome.
    Coto E; Toral JF; Menéndez MJ; Hernando I; Plasencia A; Benavides A; López-Larrea C
    Am J Med Genet; 1995 Jul; 57(3):393-6. PubMed ID: 7677140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A boy with small supernumerary marker chromosome X identified by FISH.
    Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
    Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Histologic analysis of gonadal tissue in patients with Ullrich-Turner syndrome and derivative Y chromosomes.
    Horn LC; Limbach A; Hoepffner W; Tröbs RB; Keller E; Froster UG; Richter CE; Jakubiczka S
    Pediatr Dev Pathol; 2005; 8(2):197-203. PubMed ID: 15747103
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
    Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 8.