Lv2
110 积分 2025-02-05 加入
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia
11天前
已完结
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project
14天前
已完结
Exome Sequencing Extends the Phenotypic Spectrum for ABHD12 Mutations
24天前
已完结
Genomic Landscape of Sporadic Retinitis Pigmentosa
1个月前
已完结
Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa
1年前
已完结