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

Autor:	Maria Pashchenko, Oxana Ryzhkova, F. A. Konovalov, Denis V Pyankov, T. S. Beskorovainaya, A. V. Polyakov, Nina Demina, Ilya V. Kanivets, O. A. Shchagina
Rok vydání:	2020
Předmět:	Proband Pediatrics medicine.medical_specialty Developmental and Educational Psychology medicine Autism Rett syndrome MECP2 gene medicine.disease Psychology
Zdroj:	Journal of Autism and Developmental Disorders. 51:2159-2163
ISSN:	1573-3432 0162-3257
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d8631588907cb66d24c000050d9b6db4 https://doi.org/10.1007/s10803-020-04668-0 Zobrazit plný text záznamu Full text from SpringerLink