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 *

81 related articles for article (PubMed ID: 1626622)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Genetic basis for Rett disease].
    Midro AT; Panasiuk B
    Postepy Hig Med Dosw; 1997; 51(4):399-419. PubMed ID: 9446102
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.
    Journel H; Melki J; Turleau C; Munnich A; de Grouchy J
    Am J Med Genet; 1990 Jan; 35(1):142-7. PubMed ID: 2301467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Another model for the inheritance of Rett syndrome.
    Bühler EM; Malik NJ; Alkan M
    Am J Med Genet; 1990 May; 36(1):126-31. PubMed ID: 2333902
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Skewed X chromosome inactivation failed to explain the normal phenotype of a carrier female with MECP2 mutation resulting in Rett syndrome.
    Takahashi S; Ohinata J; Makita Y; Suzuki N; Araki A; Sasaki A; Murono K; Tanaka H; Fujieda K
    Clin Genet; 2008 Mar; 73(3):257-61. PubMed ID: 18190595
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
    Ellison KA; Roth EJ; McCabe ER; Chinault AC; Zoghbi HY
    Am J Med Genet; 1993 Nov; 47(7):1124-34. PubMed ID: 8291533
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Current status of genetic research in Rett syndrome.
    Anvret M; Zhang ZP
    Neuropediatrics; 1995 Apr; 26(2):88-9. PubMed ID: 7566463
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Segregation analysis of the X-chromosome in a family with Rett syndrome in two generations.
    Anvret M; Wahlström J; Skogsberg P; Hagberg B
    Am J Med Genet; 1990 Sep; 37(1):31-5. PubMed ID: 2240040
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An explanation for another familial case of Rett syndrome: maternal germline mosaicism.
    Venâncio M; Santos M; Pereira SA; Maciel P; Saraiva JM
    Eur J Hum Genet; 2007 Aug; 15(8):902-4. PubMed ID: 17440498
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 18q-mosaicism associated with Rett syndrome phenotype.
    Gordon K; Siu VM; Sergovich F; Jung J
    Am J Med Genet; 1993 Apr; 46(2):142-4. PubMed ID: 8484399
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetics and Rett syndrome.
    Anvret M; Clarke A
    Eur Child Adolesc Psychiatry; 1997; 6 Suppl 1():89-90. PubMed ID: 9452928
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic basis of Rett syndrome.
    Van den Veyver IB; Zoghbi HY
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):82-6. PubMed ID: 12112732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Rett's syndrome. Clinical features and advances in genetics].
    Temudo T; Maciel P
    Rev Neurol; 2002 Feb; 34 Suppl 1():S54-8. PubMed ID: 12447790
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rett syndrome: the Swedish Genealogic Research Project. New data and present position.
    Akesson HO
    Eur Child Adolesc Psychiatry; 1997; 6 Suppl 1():96-8. PubMed ID: 9452929
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Analysis of the most frequent mutations in girls with Rett syndrome].
    Rosipal R; Zeman J; Hadac J; Misovicová N; Nevsímalová S; Martásek P
    Cas Lek Cesk; 2001 Aug; 140(15):473-6. PubMed ID: 11569169
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.