Rett Syndrome: Confirmation of X-Linked Dominant Inheritance, and Localization of the Gene to Xq28
- 1 November 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (5) , 1552-1557
- https://doi.org/10.1086/302105
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.Journal of Medical Genetics, 1998
- A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivationNature Genetics, 1997
- A New Rett Syndrome Family Consistent with X-Linked Inheritance Expands the X Chromosome Exclusion MapAmerican Journal of Human Genetics, 1997
- Familial Skewed X Inactivation: A Molecular Trait Associated with High Spontaneous-Abortion Rate Maps to Xq28American Journal of Human Genetics, 1997
- Rett syndrome: A disorder affecting early brain growthAnnals of Neurology, 1997
- Genetic counseling of isolated carriers of Duchenne muscular dystrophyAmerican Journal of Medical Genetics, 1996
- A 2D crossover–based map of the human X chromosome as a model for map integrationNature Genetics, 1995
- Patterns of X chromosome inactivation in the rett syndromeBrain & Development, 1990