| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3084729 | Pediatric Neurology | 2015 | 6 Pages |
Abstract
We propose that the constellation of clinical features in this child represents a novel microdeletion syndrome and hypothesize that CSPP1 or other genes within the deleted region contribute to the cerebellar development.
Keywords
Related Topics
Life Sciences
Neuroscience
Developmental Neuroscience
Authors
Dylan MB, ChB, Bergithe E. PhD, Alisha BSc(hons), Danika MBBS, Wendy BMedLabSc, Hamish PhD, Christopher MBBS,