Lv4
520 积分 2023-05-04 加入
Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes
10个月前
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
11个月前
已完结
Expression of Atoh1 , Gfi1 , and Pou4f3 in the mature cochlea reprograms nonsensory cells into hair cells
11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
11个月前
已完结
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
11个月前
已完结
Identification of a Novel CNV at 8q13 in a Family With Branchio‐Oto‐Renal Syndrome and Epilepsy
1年前
已完结
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2
1年前
已完结
Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes
1年前
已完结
Molecular diagnostics for hereditary hearing loss in children
1年前
已完结
Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing
1年前
已完结
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