Lv22
120 积分 2023-11-09 加入
Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy
8小时前
已关闭
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study
1个月前
已完结
TMEM151A phenotypic spectrum includes paroxysmal kinesigenic dyskinesia with infantile convulsions
1个月前
已完结
Digestive System Diseases, Genetic Risk, and Incident Dementia: A Prospective Cohort Study
2个月前
已完结
The genetics and pathogenesis of CAKUT
2个月前
已完结
Genetics of Chronic Kidney Disease
2个月前
已完结
Congenital adrenal hyperplasia
3个月前
已完结
Congenital adrenal hyperplasia
3个月前
已完结
Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort
4个月前
已完结
皖公网安备34019202002308
