The rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture
- 1 January 1990
- journal article
- Published by Elsevier in Brain & Development
- Vol. 12 (1), 128-130
- https://doi.org/10.1016/s0387-7604(12)80193-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Rett syndrome: Epidemiology and nosology — progress in knowledge 1986 — A conference communicationBrain & Development, 1987
- The effect of caffeine on fragile X expressionHuman Genetics, 1986
- Chromosome findings in the rett syndrome and a test of a two-step mutation theoryAmerican Journal of Medical Genetics, 1986
- Rett Syndrome: A suggested staging system for describing impairment profile with increasing age towards adolescenceAmerican Journal of Medical Genetics, 1986
- Rett syndrome: Lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutationsAmerican Journal of Medical Genetics, 1986
- Chromosome studies in 10 patients with the rett syndromeAmerican Journal of Medical Genetics, 1986
- Genetic implications of rett syndromeBrain & Development, 1985
- FRA(X)(p22) NOT ASSOCIATED WITH INFANTILE AUTISMThe Lancet, 1984
- Constitutive Fragile Sites and CancerScience, 1984
- INFANTILE AUTISM AND RETT'S SYNDROME: COMMON CHROMOSOMAL DENOMINATORThe Lancet, 1984