Rett syndrome: random X chromosome inactivation
- 1 May 1994
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 45 (5), 274-275
- https://doi.org/10.1111/j.1399-0004.1994.tb04157.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Rett syndrome: A search for gene sourcesAmerican Journal of Medical Genetics, 1992
- Segregation analysis of the X‐chromosome in a family with rett syndrome in two generationsAmerican Journal of Medical Genetics, 1990
- Patterns of X chromosome inactivation in the rett syndromeBrain & Development, 1990
- The rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte cultureBrain & Development, 1990
- A de novo X; 3 translocation in Rett syndromeAmerican Journal of Medical Genetics, 1990
- Rett phenotype with X/autosome translocation: Possible mapping to the short arm of chromosome XAmerican Journal of Medical Genetics, 1990
- Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22Genomics, 1989
- MECHANISMS OF X-CHROMOSOME REGULATIONAnnual Review of Genetics, 1988
- RETT'S SYNDROME AND ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCYThe Lancet, 1987
- CpG-rich islands and the function of DNA methylationNature, 1986