Lv1
10 积分 2024-07-22 加入
Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration
9个月前
已完结
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies
9个月前
已完结
Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss
9个月前
已完结
Family trio-based sequencing in 404 sporadic bilateral hearing loss patients discovers recessive and De novo genetic variants in multiple ways
9个月前
已完结
Challenges of Accuracy in Germline Clinical Sequencing Data
9个月前
已完结
Ivonescimab Plus Chemotherapy in Non–Small Cell Lung Cancer With EGFR Variant
9个月前
已完结
皖公网安备34019202002308
