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Search Results - Dimitropoulou, Danai
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De novo TBR1 mutations in sporadic autism disrupt protein functions
by
Deriziotis, Pelagia
,
O’Roak, Brian J.
,
Graham, Sarah A.
,
Estruch, Sara B.
,
Dimitropoulou, Danai
,
Bernier, Raphael A.
,
Gerdts, Jennifer
,
Shendure, Jay
,
Eichler, Evan E.
,
Fisher, Simon E.
Published in
Nature communications
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Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
by
Sollis, Elliot
,
Graham, Sarah A
,
Vino, Arianna
,
Froehlich, Henning
,
Vreeburg, Maaike
,
Dimitropoulou, Danai
,
Gilissen, Christian
,
Pfundt, Rolph
,
Rappold, Gudrun A
,
Brunner, Han G
,
Deriziotis, Pelagia
,
Fisher, Simon E
Published in
Human molecular genetics
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