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亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!
pudding
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2023-05-04 加入
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Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes
19天前
已完结
Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han
1个月前
已完结
Expression of Atoh1 , Gfi1 , and Pou4f3 in the mature cochlea reprograms nonsensory cells into hair cells
1个月前
已完结
Knockdown and mutation of Pou4f3 gene mutation promotes pyroptosis of cochleae in cisplatin-induced deafness mice by NLRP3/caspase-3/GSDME pathway
1个月前
已完结
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
1个月前
已完结
Identification of a Novel CNV at 8q13 in a Family With Branchio‐Oto‐Renal Syndrome and Epilepsy
2个月前
已完结
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2
2个月前
已完结
Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes
2个月前
已完结
Molecular diagnostics for hereditary hearing loss in children
3个月前
已完结
Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing
3个月前
已完结
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