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110 积分 2025-02-05 加入
PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
6小时前
求助中
Clinical Findings and Molecular Genetics of USH1C -Associated Usher Syndrome
16天前
已完结
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia
3个月前
已完结
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project
3个月前
已完结
Exome Sequencing Extends the Phenotypic Spectrum for ABHD12 Mutations
3个月前
已完结
Genomic Landscape of Sporadic Retinitis Pigmentosa
4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
Rationa lLigand-Mediated Microenvironment Regulationin Trinuclear Cu-Based Metal-Covalent Organic Frameworks for Enhanced Electrocatalytic CO Reduction
16天前
已采纳
DHDM: An interpretable masked deep‐learning model for hail potential forecasting
3个月前
已采纳
Unveiling the mechanisms of Inonotus hispidus against polycystic ovary syndrome: An integrated metabolomics and network pharmacology approach in vivo and vitro
3个月前
已采纳
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