Detalles de la búsqueda
1.
Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 978-984, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-271630
2.
Analysis of genotype-phenotype correlation for GJB2 in 221 non-syndromic deafness probands and their pedigrees / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 991-995, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-271628
3.
Molecular mechanisms underlying function of hair bundle: study on genetic deafness in mouse models / 生理学报
Acta Physiologica Sinica
; (6): 481-488, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-333175
4.
Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 382-387, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-295474
5.
Mitochondrial 12S rRNA variants studies in 456 subjects with hearing loss in seven schools for deaf and mutes in Zhejiang province / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 996-1003, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-262422
Resultados
1 -
5
de 5
1
Próxima >
>>