Lv1
20 积分 2024-01-20 加入
Phenotypic Variants of the Deafness-Associated Mitochondrial DNA A7445G Mutation
5个月前
已完结
Clinical and Genetic Features in Two Families With MELAS and the T3271C Mutation in Mitochondrial DNA
5个月前
已完结
A MERRF/MELAS Overlap Syndrome Associated with a New Point Mutation in the Mitochondrial DNA tRNA^Lys Gene
6个月前
已关闭
Molecular Epidemiology of Childhood Mitochondrial Encephalomyopathies in a Finnish Population: Sequence Analysis of Entire mtDNA of 17 Children Reveals Heteroplasmic Mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) Genes
6个月前
已完结
Telomere-to-telomere sheep genome assembly identifies variants associated with wool fineness
6个月前
已完结
Ironies of success: a new history of the American health care "system"
6个月前
已关闭
Application of the PGT-M strategy using single sperm and/or affected embryos as probands for linkage analysis in males with hereditary tumor syndromes without family history
8个月前
已完结
Comprehensive Assays for Incontinentia Pigmenti Using Long-Read Sequencing and Its Application in Preimplantation Genetic Testing
10个月前
已完结
The −KTS splice variant of WT1 is essential for ovarian determination in mice
11个月前
已完结
Chromatin accessibility landscape of mouse early embryos revealed by single-cell NanoATAC-seq2
11个月前
已完结
皖公网安备34019202002308
