Ikeoluwa Osei-Owusu

3PUBLICATIONS
28CO-AUTHORS
Condensed matter characterisation technique developmentMedical infection agents (incl. prions)Adolescent health
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Publications (3)

|Jul 09, 2025
AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions.

Russell Gear, Paul Kalitsis, Melissa Glass

|Mar 07, 2024
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.

Daniel Brooks, Elizabeth Burke, Sukyeong Lee

|Dec 18, 2020
Characterization of an unbalanced translocation causing 3q28qter duplication and 10q26.2qter deletion in a patient with global developmental delay and self-injury.

Ikeoluwa A Osei-Owusu, Alexis L Norris, Anya T Joynt

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Frequent Collaborators

1 joint publications

Alexis L Norris

1 joint publications

Jeremy Thorpe

1 joint publications

Soonweng Cho

1 joint publications

Louis Hagopian