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.
78 related articles for article (PubMed ID: 7770130)
1. Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms? Anvret M; Zhang ZP; Hagberg B Neuropediatrics; 1994 Dec; 25(6):323-4. PubMed ID: 7770130 [TBL] [Abstract][Full Text] [Related]
2. Rett syndrome studies of natural history and search for a genetic marker. Naidu S; Hyman S; Harris EL; Narayanan V; Johns D; Castora F Neuropediatrics; 1995 Apr; 26(2):63-6. PubMed ID: 7566454 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy. Nectoux J; Girard B; Bahi-Buisson N; Prieur F; Afenjar A; Rosas-Vargas H; Chelly J; Bienvenu T Pediatr Neurol; 2007 Oct; 37(4):270-4. PubMed ID: 17903671 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. [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]
10. Analysis of the genomic structure of the human glycine receptor alpha2 subunit gene and exclusion of this gene as a candidate for Rett syndrome. Cummings CJ; Dahle EJ; Zoghbi HY Am J Med Genet; 1998 Jun; 78(2):176-8. PubMed ID: 9674912 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients. Santos M; Temudo T; Kay T; Carrilho I; Medeira A; Cabral H; Gomes R; Lourenço MT; Venâncio M; Calado E; Moreira A; Oliveira G; Maciel P J Child Neurol; 2009 Jan; 24(1):49-55. PubMed ID: 19168818 [TBL] [Abstract][Full Text] [Related]
14. Preserved speech variant is allelic of classic Rett syndrome. De Bona C; Zappella M; Hayek G; Meloni I; Vitelli F; Bruttini M; Cusano R; Loffredo P; Longo I; Renieri A Eur J Hum Genet; 2000 May; 8(5):325-30. PubMed ID: 10854091 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. MECP2 mutations in Serbian Rett syndrome patients. Djarmati A; Dobricić V; Kecmanović M; Marsh P; Jancić-Stefanović J; Klein C; Djurić M; Romac S Acta Neurol Scand; 2007 Dec; 116(6):413-9. PubMed ID: 17986102 [TBL] [Abstract][Full Text] [Related]
18. Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome. Matarazzo MR; De Bonis ML; Vacca M; Della Ragione F; D'Esposito M Int J Biochem Cell Biol; 2009 Jan; 41(1):117-26. PubMed ID: 18786650 [TBL] [Abstract][Full Text] [Related]
19. Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p. Wahlström J; Uller A; Johannesson T; Holmqvist D; Darnfors C; Vujic M; Tonnby B; Hagberg B; Martinsson T J Med Genet; 1999 Apr; 36(4):343-5. PubMed ID: 10227408 [TBL] [Abstract][Full Text] [Related]
20. Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders. Wong VC; Li SY J Child Neurol; 2007 Dec; 22(12):1397-400. PubMed ID: 18174559 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]