Browse Dataset Files
Whole-exome sequencing of additional thyroid disease cases (2017-05-11)
|EGAD00001003331||Illumina HiSeq 2000,Illumina HiSeq 2500||78|
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.