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Zespół łamliwego Chromosomu X i Choroby FMR1-zależne - Postępowanie Diagnostyczne Na Podstawie Doświadczeń własnych

The presence of dynamic mutation in the FMR1 gene localized on the X chromosome (Xq28) is the major cause of Fragile X syndrome. As this syndrome is quite frequently diagnosed in patients with intellectual disability and autism spectrum disorders, the genetic testing of the FMR1 gene is a routine pr...

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Detalles Bibliográficos
Autores principales:	Landowska, Aleksandra, Rzońca, Sylwia, Bal, Jerzy, Gos, Monika
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sciendo 2018
Materias:	Original articles/Prace oryginalne
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522923/ https://www.ncbi.nlm.nih.gov/pubmed/29641418 http://dx.doi.org/10.34763/devperiodmed.20182201.2232

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