|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis显示文摘 | Oonk AM Leijendeckers JM Lammers EM Weegerink NJ Oostrik J Beynon AJ Huygen PL Kunst HP Kremer H Snik AF Pennings RJ | | 0，，： | 1 |
| 2 | Next-generation sequenc-ing identifies mutations of SMPX,which encodes the small mus-cle protein,X-linked,as a cause of progressive hearing impair-ment显示文摘 | Schraders M Haas SA Weegerink NJ Oostrik J Hu H Hoefsloot LH Kannan S Huygen PL Pennings RJ Admiraal RJ Kalscheuer VM Kunst HP Kremer H | | 0，，： | 1 |
| 3 | Next-generation sequencing identifies mutations of SMPX,which encodes the small muscle protein,Xlinked,as a cause of progressive hearing impairment显示文摘 | SCHRADERS M HAAS S A WEEGERINK N J D | 2011 | Am J Hum Genet2011，88，： | 1 |
| 4 | Audiometric characteristics of aDutch family with Muckle-Wells syndrome显示文摘 | Weegerink NJ Schraders M Leijendeckers J | 2011 | Hear Res2011，282，12： | 1 |
| 5 | Next-genera- tion sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progres- sive hearing impairment显示文摘 | Schraders M Haas SA Weegerink NJ | 2011 | Am J Hum Genet2011，88，： | 1 |
| 6 | Genotype-phe- notype correlation in DFNB8/10 families with TMPRSS3 muta- tions显示文摘 | Weegerink NJ Schraders M Oostrik J | 2011 | J Assoc Res Otolaryngol2011，12，6： | 1 |
| 7 | Next--genera- tion sequencing identifies mutations of SMPX, which encodes the small muscle protein, X--linked, as a cause of progres- sive hearing impairment显示文摘 | Schraders M Haas SA Weegerink NJ | 2011 | Am J Hum Genet2011，88，： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员