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Items: 1 to 20 of 39

1.

Mutations and polymorphisms in the human methyl CpG-binding protein MECP2.

Miltenberger-Miltenyi G, Laccone F.

Hum Mutat. 2003 Aug;22(2):107-15. Review.

PMID:
12872250
2.

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.

Amir RE, Zoghbi HY.

Am J Med Genet. 2000 Summer;97(2):147-52. Review.

PMID:
11180222
3.

Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.

Van den Veyver IB, Zoghbi HY.

Brain Dev. 2001 Dec;23 Suppl 1:S147-51. Review.

PMID:
11738862
4.

MeCP2 and other methyl-CpG binding proteins.

Jørgensen HF, Bird A.

Ment Retard Dev Disabil Res Rev. 2002;8(2):87-93. Review.

PMID:
12112733
5.

Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).

Moog U, Smeets EE, van Roozendaal KE, Schoenmakers S, Herbergs J, Schoonbrood-Lenssen AM, Schrander-Stumpel CT.

Eur J Paediatr Neurol. 2003;7(1):5-12. Review.

PMID:
12615169
6.

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. Review.

PMID:
12112735
7.

Rethinking the fate of males with mutations in the gene that causes Rett syndrome.

Schanen C.

Brain Dev. 2001 Dec;23 Suppl 1:S144-6. Review.

PMID:
11738861
8.

MeCP2 in neurons: closing in on the causes of Rett syndrome.

Caballero IM, Hendrich B.

Hum Mol Genet. 2005 Apr 15;14 Spec No 1:R19-26. Review. Erratum in: Hum Mol Genet. 2005 Jul 15;14(14):2089.

PMID:
15809268
9.

Rett syndrome: from the gene to the disease.

Matijevic T, Knezevic J, Slavica M, Pavelic J.

Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24. Review.

10.

Methyl-CpG-binding protein 2 mutations in Rett syndrome.

Van den Veyver IB, Zoghbi HY.

Curr Opin Genet Dev. 2000 Jun;10(3):275-9. Review.

PMID:
10826991
11.
13.

Rett syndrome: clinical correlates of the newly discovered gene.

Percy AK.

Brain Dev. 2001 Dec;23 Suppl 1:S202-5. Review.

PMID:
11738873
14.
15.

Rett syndrome: of girls and mice--lessons for regression in autism.

Glaze DG.

Ment Retard Dev Disabil Res Rev. 2004;10(2):154-8. Review.

PMID:
15362175
16.

Genetic basis of Rett syndrome.

Van den Veyver IB, Zoghbi HY.

Ment Retard Dev Disabil Res Rev. 2002;8(2):82-6. Review.

PMID:
12112732
17.

Rett syndrome: a prototypical neurodevelopmental disorder.

Neul JL, Zoghbi HY.

Neuroscientist. 2004 Apr;10(2):118-28. Review.

PMID:
15070486
18.

The role of X-chromosome inactivation in the manifestation of Rett syndrome.

Takagi N.

Brain Dev. 2001 Dec;23 Suppl 1:S182-5. Review.

PMID:
11738869
19.

Importance of Rett syndrome in child neurology.

Dunn HG.

Brain Dev. 2001 Dec;23 Suppl 1:S38-43. Review.

PMID:
11738840
20.

Rett syndrome: the complex nature of a monogenic disease.

Renieri A, Meloni I, Longo I, Ariani F, Mari F, Pescucci C, Cambi F.

J Mol Med (Berl). 2003 Jun;81(6):346-54. Epub 2003 May 16. Review.

PMID:
12750821

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