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
Language | Label | Description | Also known as |
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English | 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. |
scientific article published on 12 September 2012 |
Statements
14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype (English)
Carolyn J Ellaway
Gladys Ho
Elisa Bettella
Alisa Knapman
Felicity Collins
Anna Hackett
Fiona McKenzie
Artur Darmanian
Gregory B Peters
12 September 2012
1 reference