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 *

98 related articles for article (PubMed ID: 1283565)

  • 1. 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]  

  • 2. Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother.
    Panasiuk B; Midro AT; Zadrozna-Tołwińska B
    Clin Genet; 1997 Aug; 52(2):120-5. PubMed ID: 9298748
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Alterations in replication timing of X-chromosome bands in Rett syndrome.
    Kormann-Bortolotto MH; Webb T
    J Intellect Disabil Res; 1995 Apr; 39 ( Pt 2)():91-6. PubMed ID: 7787387
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. In search of a genetic basis for the Rett syndrome.
    Martinho PS; Otto PG; Kok F; Diament A; Marques-Dias MJ; Gonzalez CH
    Hum Genet; 1990 Dec; 86(2):131-4. PubMed ID: 2265825
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. A de novo X;3 translocation in Rett syndrome.
    Zoghbi HY; Ledbetter DH; Schultz R; Percy AK; Glaze DG
    Am J Med Genet; 1990 Jan; 35(1):148-51. PubMed ID: 2301468
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases.
    Vorsanova SG; Demidova IA; Ulas VYu ; Soloviev IV; Kazantzeva LZ; Yurov YuB
    Neuroreport; 1996 Dec; 8(1):187-9. PubMed ID: 9051778
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cytogenetic and molecular genetic diagnostics of Rett syndrome in children].
    Vorsanova SG; Demidova IA; Ulas VIu; Solov'ev IV; Kravets VS; Kazantseva LZ; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 1998; 98(4):53-6. PubMed ID: 9606901
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Is Rett syndrome a chromosome breakage syndrome?
    Telvi L; Leboyer M; Chiron C; Feingold J; Ponsot G
    Am J Med Genet; 1994 Jul; 51(4):602-5. PubMed ID: 7943047
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rett syndrome: random X chromosome inactivation.
    Anvret M; Wahlström J
    Clin Genet; 1994 May; 45(5):274-5. PubMed ID: 8076417
    [No Abstract]   [Full Text] [Related]  

  • 18. A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease.
    Rosenberg C; Wouters CH; Szuhai K; Dorland R; Pearson P; Poll-The BT; Colombijn RM; Breuning M; Lindhout D
    Eur J Hum Genet; 2001 Mar; 9(3):171-7. PubMed ID: 11313755
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.
    Auranen M; Vanhala R; Vosman M; Levander M; Varilo T; Hietala M; Riikonen R; Peltonen L; Järvelä I
    Neurology; 2001 Mar; 56(5):611-7. PubMed ID: 11245712
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.