Whole genome analysis of an extended pedigree with Prader-Willi Syndrome, Hereditary Hemochromatosis, Familial Dysautonomia, Tourette Syndrome and other illnesses

Fang, Han, Lyon, Gholson J. (2014) Whole genome analysis of an extended pedigree with Prader-Willi Syndrome, Hereditary Hemochromatosis, Familial Dysautonomia, Tourette Syndrome and other illnesses. In: Cold Spring Harbor Laboratory Personal Genomes Meeting, November 2014, Cold Spring Harbor, NY. (Unpublished)

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Item Type: Conference or Workshop Item (Poster)
Subjects: bioinformatics
diseases & disorders
bioinformatics > genomics and proteomics
Investigative techniques and equipment > assays > whole genome sequencing
CSHL Authors:
Communities: CSHL labs > Lyon lab
Depositing User: Andrea Potopsingh
Date Deposited: 11 Nov 2014 19:52
Last Modified: 11 Nov 2014 19:52
URI: http://repository.cshl.edu/id/eprint/30908

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