Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys)
- 1 December 2001
- journal article
- case report
- Published by Elsevier in Brain & Development
- Vol. 23, S196-S201
- https://doi.org/10.1016/s0387-7604(01)00347-3
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes: Rapid chromosome identification by directly fluorescently labeled alphoid DNA probesHuman Genetics, 1996
- X chromosome inactivation in 30 girls with Rett syndrome: Analysis using the probeHuman Genetics, 1996
- Rett variants: A suggested model for inclusion criteriaPediatric Neurology, 1994
- In search of a genetic basis for the Rett syndromeHuman Genetics, 1990
- Another model for the inheritance of Rett syndromeAmerican Journal of Medical Genetics, 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
- Diagnostic criteria for rett syndromeAnnals of Neurology, 1988
- A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 casesAnnals of Neurology, 1983
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971