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Whole-exome sequencing of additional thyroid disease cases (2017-05-11)

Dataset ID Technology Samples
EGAD00001003331 Illumina HiSeq 2000,Illumina HiSeq 2500 78

Dataset Description

Whole-exome sequencing of a cohort of families (probands and affected/unaffected relatives) suffering from one of two rare thyroid disorders: congenital hypothyroidism (CH) and resistance to thyroid hormone (RTH). This dataset contains all the data available for this study on 2017-05-11.