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.
106 related articles for article (PubMed ID: 2240040)
1. 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]
2. Rett-like syndrome in fragile X syndrome. Alembik Y; Dott B; Stoll C Genet Couns; 1995; 6(3):207-10. PubMed ID: 8588847 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3). Gustavsson P; Kimber E; Wahlström J; Annerén G Am J Med Genet; 1999 Feb; 82(4):348-51. PubMed ID: 10051171 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome. Yaron Y; Ben Zeev B; Shomrat R; Bercovich D; Naiman T; Orr-Urtreger A Hum Mutat; 2002 Oct; 20(4):323-4. PubMed ID: 12325033 [TBL] [Abstract][Full Text] [Related]
7. Trisomy 21 and Rett syndrome: a double burden. Leonard H; Weaving L; Eastaugh P; Smith L; Delatycki M; Witt Engerström I; Christodoulou J J Paediatr Child Health; 2004 Jul; 40(7):406-9. PubMed ID: 15228575 [TBL] [Abstract][Full Text] [Related]
8. 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]
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. 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]
11. 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]
12. Homozygosity for MECP2 gene in a girl with classical Rett syndrome. Karall D; Haberlandt E; Scholl-Bürgi S; Baumgartner S; Naudó M; Martorell L Eur J Med Genet; 2007; 50(6):465-8. PubMed ID: 17881312 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. [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]
18. 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]
19. Rett syndrome: a search for gene sources. Akesson HO; Hagberg B; Wahlström J; Engerström IW Am J Med Genet; 1992 Jan; 42(1):104-8. PubMed ID: 1308347 [TBL] [Abstract][Full Text] [Related]
20. [Rett syndrome. A report of fifteen cases]. Echenne B; Bressot N; Cheminal R; Van Leuwen F; Compagnon P; Azaïs M Ann Pediatr (Paris); 1989 Dec; 36(10):661-8. PubMed ID: 2533856 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]