Lyon, Gholson J. (January 2016) A rare genetic “transcriptomopathy” syndrome leading to insights into more common neurologic disorders. In: New York City Wide Human Genetics Meeting 2016, Rockefeller University, New York City, NY. (Unpublished)
| Item Type: | Conference or Workshop Item (Lecture) |
|---|---|
| Subjects: | bioinformatics diseases & disorders > congenital hereditary genetic diseases bioinformatics > genomics and proteomics diseases & disorders > congenital hereditary genetic diseases > mental retardation |
| CSHL Authors: | |
| Communities: | CSHL labs > Lyon lab |
| Depositing User: | Stephanie Hovanec |
| Date: | January 2016 |
| Date Deposited: | 11 May 2016 16:37 |
| Last Modified: | 11 May 2016 16:37 |
| URI: | https://repository.cshl.edu/id/eprint/32792 |
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