| Literature DB >> 3832947 |
Abstract
Cytogenetic analysis in 14 girls with the Rett syndrome revealed a deletion on the short arm of the X chromosome (del(X) (pter;p22] in one, and a fragile site on chromosome Xp22 in six of the girls. Two hypotheses concerning the genetic background to the Rett syndrome are suggested; an X-linked dominant mutation theory and a two-step mutation theory.Entities:
Mesh:
Year: 1985 PMID: 3832947 DOI: 10.1016/s0387-7604(85)80003-6
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961