14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. (Q36809678)

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scientific article published on 12 September 2012
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14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
scientific article published on 12 September 2012

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    14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype (English)

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