These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 8566963)

  • 1. X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe.
    Camus P; Abbadi N; Perrier MC; Chéry M; Gilgenkrantz S
    Hum Genet; 1996 Feb; 97(2):247-50. PubMed ID: 8566963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X chromosome-inactivation patterns in patients with Rett syndrome.
    Krepischi AC; Kok F; Otto PG
    Hum Genet; 1998 Mar; 102(3):319-21. PubMed ID: 9544845
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X inactivation in Rett syndrome: a preliminary study showing partial preferential inactivation of paternal X with the M27 beta probe.
    Camus P; Abbadi N; Gilgenkrantz S
    Am J Med Genet; 1994 Apr; 50(3):307-8. PubMed ID: 8042680
    [No Abstract]   [Full Text] [Related]  

  • 4. Patterns of X chromosome inactivation in the Rett syndrome.
    Zoghbi HY; Percy AK; Schultz RJ; Fill C
    Brain Dev; 1990; 12(1):131-5. PubMed ID: 2344009
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome.
    Webb T; Watkiss E; Woods CG
    Clin Genet; 1993 Nov; 44(5):236-40. PubMed ID: 7906210
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A comparative study of X-inactivation in Rett syndrome probands and control subjects.
    Webb T; Watkiss E
    Clin Genet; 1996 Apr; 49(4):189-95. PubMed ID: 8828984
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.
    Migeon BR; Dunn MA; Thomas G; Schmeckpeper BJ; Naidu S
    Am J Hum Genet; 1995 Mar; 56(3):647-53. PubMed ID: 7887418
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
    Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome.
    Yurov YB; Vorsanova SG; Kolotii AD; Iourov IY
    Brain Dev; 2001 Dec; 23 Suppl 1():S214-7. PubMed ID: 11738875
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].
    Jiang SL; Bao XH; Song FY; Pan H; Li MR; Wu XR
    Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):648-52. PubMed ID: 17217653
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-inactivation in girls with Rett syndrome.
    Kormann-Bortolotto MH; Woods CG; Green SH; Webb T
    Clin Genet; 1992 Dec; 42(6):296-301. PubMed ID: 1283565
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probe.
    Goodship J; Carter J; Espanol T; Boyd Y; Malcolm S; Levinsky RJ
    Blood; 1991 Jun; 77(12):2677-81. PubMed ID: 2043768
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.
    Villard L; Lévy N; Xiang F; Kpebe A; Labelle V; Chevillard C; Zhang Z; Schwartz CE; Tardieu M; Chelly J; Anvret M; Fontès M
    J Med Genet; 2001 Jul; 38(7):435-42. PubMed ID: 11432961
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndrome.
    Vorsanova SG; Yurov YB; Kolotii AD; Soloviev IV
    Brain Dev; 2001 Dec; 23 Suppl 1():S191-5. PubMed ID: 11738871
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27 beta): correlation with X-inactivation status.
    Boyd Y; Fraser NJ
    Genomics; 1990 Jun; 7(2):182-7. PubMed ID: 1693357
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.
    Allen RC; Zoghbi HY; Moseley AB; Rosenblatt HM; Belmont JW
    Am J Hum Genet; 1992 Dec; 51(6):1229-39. PubMed ID: 1281384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Rett Syndrome: the recent advances in genetic studies in the USA.
    Percy AK
    Brain Dev; 1992 May; 14 Suppl():S104-5. PubMed ID: 1626622
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.
    Schanen NC; Dahle EJ; Capozzoli F; Holm VA; Zoghbi HY; Francke U
    Am J Hum Genet; 1997 Sep; 61(3):634-41. PubMed ID: 9326329
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].
    Zhu XW; Pan H; Li MR; Bao XH; Zhang JJ; Wu XR
    Zhonghua Er Ke Za Zhi; 2009 Aug; 47(8):565-9. PubMed ID: 19951486
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Increased skewing of X chromosome inactivation in Rett syndrome patients and their mothers.
    Knudsen GP; Neilson TC; Pedersen J; Kerr A; Schwartz M; Hulten M; Bailey ME; Orstavik KH
    Eur J Hum Genet; 2006 Nov; 14(11):1189-94. PubMed ID: 16823396
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.