A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms
2015 · Molecular Cytogenetics · 66 citations
https://doi.org/10.1186/s13039-015-0157-0
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Vesna Bryn
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Vesna Bryn is an academic researcher from Innlandet Hospital Trust. The author has contributed to research in topics: Autism Spectrum Disorder Research & Child Nutrition and Feeding Issues & Genetics and Neurodevelopmental Disorders. The author has an h-index of 8, co-authored 8 publications.
ORCID: 0000-0002-8359-2990Papers by this author
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