Investigating genetic etiology and exploring clinical value of whole-exome sequencing in congenital hypothyroidism
收藏DataCite Commons2021-01-25 更新2024-07-28 收录
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https://figshare.com/articles/dataset/Investigating_the_genetic_etiology_of_congenital_hypothyroidism_and_the_clinical_value_of_whole-exome_sequencing_in_newborn_screening/13636343/2
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资源简介：
We performed whole-exome sequencing in 233 patients with congenital hypothyroidism to investigate the genetic etiology of congenital hypothyroidism and the clinical value of whole-exome sequencing in newborn screening.
提供机构：
figshare
创建时间：
2021-01-25
