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Did you mean: person:("solis, E.") • person:("hollis, E.") • person:("soltis, E.")
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Functional characterization of TBR1 variants in neurodevelopmental disorder
Free accessBASE | 2018| -
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstruction
British Library Online Contents | 2018| -
P3.32 The molecular genetics of monogenic neuromuscular disorders characterised by reduced foetal movement
British Library Online Contents | 2011| -
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
British Library Online Contents | 2016| -
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders
British Library Online Contents | 2018|
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