A rare genetic “transcriptomopathy” syndrome leading to insights into more common neurologic disorders

Lyon, Gholson J. (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 (Unpublished)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 Deposited: 11 May 2016 16:37
Last Modified: 11 May 2016 16:37
URI: http://repository.cshl.edu/id/eprint/32792

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