Málstofa: Genetics

A novel mouse model to explore in utero malleability of the neurological dysfunction of Wiedemann-Steiner syndrome.

Abnormal hypoxia responses in a Kabuki syndrome chondrocyte model

SLC13A5 in the human brain – a road map to in vitro models

Systematic disruption of EM genes to understand transcriptional effect and role in neurodevelopmental disorders.

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