Höfundar: Hans Tomas Björnsson

Málstofa: Genetics

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

Salur: B

Málstofa: Genetics and diseases

A mechanistic hypothesis explaining the occurrence of two distinct phenotypes from the CREBBP/EP300 genes

Salur: B

Málstofa: Genetics

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

Salur: B

Málstofa: Genetics

Abnormal hypoxia responses in a Kabuki syndrome chondrocyte model

Salur: B

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