259 related articles for article (PubMed ID: 11913564)
1. Rett syndrome: clinical manifestations in males with MECP2 mutations.
Zeev BB; Yaron Y; Schanen NC; Wolf H; Brandt N; Ginot N; Shomrat R; Orr-Urtreger A
J Child Neurol; 2002 Jan; 17(1):20-4. PubMed ID: 11913564
[TBL] [Abstract][Full Text] [Related]
2. Mutation analysis in Rett syndrome.
Milunsky JM; Lebo RV; Ikuta T; Maher TA; Haverty CE; Milunsky A
Genet Test; 2001; 5(4):321-5. PubMed ID: 11960578
[TBL] [Abstract][Full Text] [Related]
3. A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome.
Buschdorf JP; Strätling WH
J Mol Med (Berl); 2004 Feb; 82(2):135-43. PubMed ID: 14618241
[TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome.
Chae JH; Hwang YS; Kim KJ
J Child Neurol; 2002 Jan; 17(1):33-6. PubMed ID: 11913567
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 12615169
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 12112735
[TBL] [Abstract][Full Text] [Related]
7. Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.
Topçu M; Akyerli C; Sayi A; Törüner GA; Koçoğlu SR; Cimbiş M; Ozçelik T
Eur J Hum Genet; 2002 Jan; 10(1):77-81. PubMed ID: 11896459
[TBL] [Abstract][Full Text] [Related]
8. Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome.
Amano K; Nomura Y; Segawa M; Yamakawa K
J Hum Genet; 2000; 45(4):231-6. PubMed ID: 10944854
[TBL] [Abstract][Full Text] [Related]
9. Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.
Amir RE; Zoghbi HY
Am J Med Genet; 2000; 97(2):147-52. PubMed ID: 11180222
[TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations.
Shahbazian MD; Zoghbi HY
Curr Opin Neurol; 2001 Apr; 14(2):171-6. PubMed ID: 11262731
[TBL] [Abstract][Full Text] [Related]
11. [Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis].
Bao XH; Pan H; Song FY; Wu XR
Zhonghua Er Ke Za Zhi; 2004 Apr; 42(4):252-5. PubMed ID: 15157382
[TBL] [Abstract][Full Text] [Related]
12. Rett syndrome: a prototypical neurodevelopmental disorder.
Neul JL; Zoghbi HY
Neuroscientist; 2004 Apr; 10(2):118-28. PubMed ID: 15070486
[TBL] [Abstract][Full Text] [Related]
13. The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
Hammer S; Dorrani N; Dragich J; Kudo S; Schanen C
Ment Retard Dev Disabil Res Rev; 2002; 8(2):94-8. PubMed ID: 12112734
[TBL] [Abstract][Full Text] [Related]
14. No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.
Vourc'h P; Bienvenu T; Beldjord C; Chelly J; Barthélémy C; Müh JP; Andres C
Eur J Hum Genet; 2001 Jul; 9(7):556-8. PubMed ID: 11464249
[TBL] [Abstract][Full Text] [Related]
15. MECP2 and beyond: phenotype-genotype correlations in Rett syndrome.
Christodoulou J; Weaving LS
J Child Neurol; 2003 Oct; 18(10):669-74. PubMed ID: 14649547
[TBL] [Abstract][Full Text] [Related]
16. Classic Rett syndrome in a boy with R133C mutation of MECP2.
Masuyama T; Matsuo M; Jing JJ; Tabara Y; Kitsuki K; Yamagata H; Kan Y; Miki T; Ishii K; Kondo I
Brain Dev; 2005 Sep; 27(6):439-42. PubMed ID: 16122633
[TBL] [Abstract][Full Text] [Related]
17. Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.
Huppke P; Laccone F; Krämer N; Engel W; Hanefeld F
Hum Mol Genet; 2000 May; 9(9):1369-75. PubMed ID: 10814718
[TBL] [Abstract][Full Text] [Related]
18. De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia.
Kleefstra T; Yntema HG; Oudakker AR; Romein T; Sistermans E; Nillessen W; van Bokhoven H; de Vries BB; Hamel BC
Clin Genet; 2002 May; 61(5):359-62. PubMed ID: 12081720
[TBL] [Abstract][Full Text] [Related]
19. MECP2 mutations account for most cases of typical forms of Rett syndrome.
Bienvenu T; Carrié A; de Roux N; Vinet MC; Jonveaux P; Couvert P; Villard L; Arzimanoglou A; Beldjord C; Fontes M; Tardieu M; Chelly J
Hum Mol Genet; 2000 May; 9(9):1377-84. PubMed ID: 10814719
[TBL] [Abstract][Full Text] [Related]
20. A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 gene.
Bzduch V; Zahorakova D; Grechanina E; Zdibskaja EP; Goldfarb IG; Zeman J; Martasek P
Bratisl Lek Listy; 2004; 105(9):299-302. PubMed ID: 15633890
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]