Lyon, Gholson J. (October 2015) Variants in TAF1 are associated with a new syndrome with severe intellectual disability and characteristic dysmorphic features. In: he American Society of Human Genetics (ASHG) 2015, Baltimore, MD. (Unpublished)
Item Type: | Conference or Workshop Item (Lecture) |
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Subjects: | bioinformatics diseases & disorders > congenital hereditary genetic diseases bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > genes, structure and function diseases & disorders > congenital hereditary genetic diseases > mental retardation Investigative techniques and equipment > assays > next generation sequencing |
CSHL Authors: | |
Communities: | CSHL labs > Lyon lab |
Depositing User: | Stephanie Hovanec |
Date: | October 2015 |
Date Deposited: | 11 May 2016 16:26 |
Last Modified: | 11 May 2016 16:26 |
URI: | https://repository.cshl.edu/id/eprint/32790 |
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