Showing 1 - 2 results of 2 for search 'Prisca Mbonu', query time: 0.02s Refine Results
  1. 1
    P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome

    P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome by Zohra Shad, Prisca Mbonu, Kelly Pagidas

    Published 2023-01-01
    Get full text
    Article
  2. 2
    P319: Expanding the phenotype of EIF3F-related neurodevelopmental disorder

    P319: Expanding the phenotype of EIF3F-related neurodevelopmental disorder by Zohra Shad, Prisca Mbonu, Isabella Aguiar, Laiba Hassan, Elena Repnikova

    Published 2024-01-01
    Get full text
    Article

Search Tools: