官方服务:
资源简介:
Pediatric hypothyroidism
儿童甲状腺功能减退症
应用场景:
创建时间:
2022-04-29
相关数据集
Targeted next-generation sequencing for congenital hypothyroidism with positive neonatal TSH screening
We performed genetic analysis of 24 causative genes using next-generation sequencing in 167 patients with congenital hypothyroidism
DataCite Commons2020-08-25 更新100
Hypoparathyroidism and Fahr’s syndrome: case series
Abstract Hypoparathyroidism (HP) is a rare metabolic disorder and causes hypocalcemia because parathyroid hormone secretion is inadequate to mobilize calcium from bone and reabsorb calcium from kidney
DataCite Commons2023-01-10 更新80
SLC5A5 mutation.xlsx
Two hundred and seventy-three patients with primary congenital hypothyroidism were screened for mutations in SLC5A5 by next-generation sequencing.
DataCite Commons2024-02-06 更新50
Hypothyroid Dataset
Dataset com informações sobre Hipotiroidismo com 30 atributos para classificação.
DataONE2020-06-24 更新90



