Literature DB >> 32816169

Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome.

Tatiana Beskorovainaya1, Fedor Konovalov2, Nina Demina3, Olga Shchagina3, Maria Pashchenko3, Ilya Kanivets4, Denis Pyankov4, Oxana Ryzhkova3, Alexander Polyakov3.   

Abstract

Entities:  

Year:  2021        PMID: 32816169     DOI: 10.1007/s10803-020-04668-0

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


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  2 in total

1.  [On a unusual brain atrophy syndrome in hyperammonemia in childhood].

Authors:  A Rett
Journal:  Wien Med Wochenschr       Date:  1966-09-10

2.  Rett syndrome: Swedish approach to analysis of prevalence and cause.

Authors:  B Hagberg
Journal:  Brain Dev       Date:  1985       Impact factor: 1.961

  2 in total

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