Literature DB >> 3087197

Chromosome findings in the Rett syndrome and a test of a two-step mutation theory.

J Wahlström, M Anvret.   

Abstract

Chromosome findings are described in 22 girls with the Rett syndrome. One of the girls had a duplication of chromosome 6, another showed a deletion X(p22----pter) in 10% of the cells from fibroblast cultures. Fragile X(p22) was seen in 9 of the 22 girls with Rett syndrome. A relationship between the disorder and fragile X(p22) could not be proven. Family data contradict our theory of a two-step mutation as the cause of the Rett syndrome.

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Year:  1986        PMID: 3087197     DOI: 10.1002/ajmg.1320250537

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  6 in total

1.  Some remarks regarding the search for a genetic basis for Rett syndrome.

Authors:  E M Bühler
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

2.  Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Authors:  N Archidiacono; M Lerone; M Rocchi; M Anvret; T Ozcelik; U Francke; G Romeo
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132

3.  In search of a genetic basis for the Rett syndrome.

Authors:  P S Martinho; P G Otto; F Kok; A Diament; M J Marques-Dias; C H Gonzalez
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

Review 4.  Rett syndrome: a review of current knowledge.

Authors:  R Van Acker
Journal:  J Autism Dev Disord       Date:  1991-12

Review 5.  Rett syndrome.

Authors:  A Clarke
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

6.  The borderland of autism and Rett syndrome: five case histories to highlight diagnostic difficulties.

Authors:  C Gillberg
Journal:  J Autism Dev Disord       Date:  1989-12
  6 in total

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