Elin Tønne

2PUBLICATIONS
2CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (2)

|Jan 26, 2022
Whole-exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways.

Elin Tønne, Bernt Johan Due-Tønnessen, Magnus Dehli Vigeland

|Dec 08, 2020
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.

Elin Tønne, Bernt Johan Due-Tønnessen, Inger-Lise Mero

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Frequent Collaborators

1 joint publications

Kristian Tveten

1 joint publications

Torstein Ragnar Meling