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)

  • 21. 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]  

  • 22. 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]  

  • 23. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.
    Amir RE; Van den Veyver IB; Schultz R; Malicki DM; Tran CQ; Dahle EJ; Philippi A; Timar L; Percy AK; Motil KJ; Lichtarge O; Smith EO; Glaze DG; Zoghbi HY
    Ann Neurol; 2000 May; 47(5):670-9. PubMed ID: 10805343
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.
    Xinhua Bao ; Shengling Jiang ; Fuying Song ; Hong Pan ; Meirong Li ; Wu XR
    J Child Neurol; 2008 Jan; 23(1):22-5. PubMed ID: 18184939
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical profile of a male with Rett syndrome.
    Budden SS; Dorsey HC; Steiner RD
    Brain Dev; 2005 Nov; 27 Suppl 1():S69-S71. PubMed ID: 16182490
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mother and daughter with Rett syndrome.
    Engerström IW; Forslund M
    Dev Med Child Neurol; 1992 Nov; 34(11):1022-3. PubMed ID: 1426681
    [No Abstract]   [Full Text] [Related]  

  • 28. [Developmental disorder in girls due to Rett syndrome].
    Pruissen DM; Sinke RJ; Terhal PA; Beemer FA; Peters AC
    Ned Tijdschr Geneeskd; 2003 Aug; 147(32):1560-3. PubMed ID: 12942847
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rett syndrome: genetic breakthrough.
    Ellaway C; Christdoulou J
    J Paediatr Child Health; 1999 Dec; 35(6):593. PubMed ID: 10633311
    [No Abstract]   [Full Text] [Related]  

  • 30. Additional clinical and cytogenetic findings associated with Rett syndrome.
    Simonic I; Gericke GS; Lippert M; Schoeman JF
    Am J Med Genet; 1997 May; 74(3):331-7. PubMed ID: 9184319
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Germline mosaicism for a MECP2 mutation in a man with two Rett daughters.
    Evans JC; Archer HL; Whatley SD; Clarke A
    Clin Genet; 2006 Oct; 70(4):336-8. PubMed ID: 16965328
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Rett syndrome: a diagnostic, clinical and molecular update].
    Tejada MI
    Rev Neurol; 2006 Jan; 42 Suppl 1():S55-9. PubMed ID: 16506134
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Prevalence study of Rett syndrome in North Dakota children.
    Burd L; Vesley B; Martsolf JT; Kerbeshian J
    Am J Med Genet; 1991 Mar; 38(4):565-8. PubMed ID: 2063900
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Rett syndrome: clinical and molecular aspects].
    Záhoráková D; Zeman J; Martásek P
    Cas Lek Cesk; 2007; 146(8):647-52. PubMed ID: 17874730
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband.
    Hardwick SA; Reuter K; Williamson SL; Vasudevan V; Donald J; Slater K; Bennetts B; Bebbington A; Leonard H; Williams SR; Smith RL; Cloosterman D; Christodoulou J
    Eur J Hum Genet; 2007 Dec; 15(12):1218-29. PubMed ID: 17712354
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndrome.
    Schollen E; Smeets E; Deflem E; Fryns JP; Matthijs G
    Hum Mutat; 2003 Aug; 22(2):116-20. PubMed ID: 12872251
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Clinical and molecular genetic findings in four girls with Rett syndrome].
    Deutscher K; Deutscher J; Bergmann L; Tefs K; Reichwald K; Schuster V
    Klin Padiatr; 2002; 214(5):291-4. PubMed ID: 12235545
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome.
    Orstavik RE; Tommerup N; Eiklid K; Orstavik KH
    Am J Med Genet; 1995 Mar; 56(2):210-4. PubMed ID: 7625447
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Rett syndrome.
    Ben Zeev Ghidoni B
    Child Adolesc Psychiatr Clin N Am; 2007 Jul; 16(3):723-43. PubMed ID: 17562589
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.