30.05.2019 · Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability (DD/ID) in all affected ...
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Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in the Yin Yang 1 (YY1) gene.
Gabriele-de Vries syndrome (GADEVS) is an autosomal dominant neurodevelopmental disorder characterized by delayed psychomotor development, ...
Clinical resource with information about Gabriele de Vries syndrome and its clinical features, YY1, available genetic tests from US and labs around the ...
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Gabriele-de Vries syndrome (GADEVS) is a recently described genetic disorder caused by the deletion of or a pathogenic variant in the YY1 transcription ...
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23.12.2020 · 1 BACKGROUND. Gabriele-de Vries syndrome (GADEVS, OMIM 617557) is a newly recognized neurodevelopmental disorder (NDD) characterized by mild-to- ...
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