Kyra Eva Stuurman

3PUBLICATIONS
3CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (3)

|Jan 12, 2020
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities.

Roya Bina, Dena Matalon, Brieana Fregeau

|May 02, 2019
Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era.

Kyra E Stuurman, Marieke Joosten, Ineke van der Burgt

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