Browse Dataset Files
Whole-exome sequencing of additional thyroid disease cases (2018-08-13)
|EGAD00001004293||Illumina HiSeq 2000,Illumina HiSeq 2500||110|
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 2018-08-13.