Literature DB >> 9606901

[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children].

S G Vorsanova, I A Demidova, V Iu Ulas, I V Solov'ev, V S Kravets, L Z Kazantseva, Iu B Iurov.   

Abstract

Rett syndrome in 32 children (31 girls and 1 boy) was diagnosed according to International association on Rett syndrome. The phenomenon of the presence of special type of late-replicating chromosome X (type C) was revealed. This phenomenon may be recommended as a diagnostic test for both preclinical periods of development of the disease and in atypical cases of Rett syndrome.

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Year:  1998        PMID: 9606901

Source DB:  PubMed          Journal:  Zh Nevrol Psikhiatr Im S S Korsakova        ISSN: 1997-7298


  4 in total

1.  Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders.

Authors:  S G Vorsanova; V Yu Voinova; I Yu Yurov; O S Kurinnaya; I A Demidova; Yu B Yurov
Journal:  Neurosci Behav Physiol       Date:  2010-09

2.  Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders.

Authors:  S G Vorsanova; I Yu Yurov; I A Demidova; V Yu Voinova-Ulas; V S Kravets; I V Solov'ev; N L Gorbachevskaya; Yu B Yurov
Journal:  Neurosci Behav Physiol       Date:  2007-07

3.  Svetlana G. Vorsanova (1945-2021).

Authors:  Ivan Y Iourov
Journal:  Mol Cytogenet       Date:  2022-08-19       Impact factor: 1.904

Review 4.  VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia.

Authors:  Ivan Y Iourov; Svetlana G Vorsanova; Yuri B Yurov; Thomas Bertrand
Journal:  Mol Cytogenet       Date:  2018-12-24       Impact factor: 2.009

  4 in total

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