Suchergebnisse - "YUAN HUIJUN"

PubPharm (14)

1

A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss

enthalten in: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery | 2016

von Zhang, D. | Duan, H. | Lin, P. | +9

2

A new method for simultaneous multi-gene mutation screening in 355 patients with nonsyndromic hearing loss of Inner Mongolia Autonomous region

enthalten in: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery | 2015

von Zhang, D. | Duan, H. | Yuan, H. | +1

3

Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people

enthalten in: Acta oto-laryngologica | 2015

von Zhu, Y. | Zhao, J. | Feng, B. | +5

4

Resolving the genetic heterogeneity of prelingual hearing loss within one family : Performance comparison and application of two targeted next generation sequencing approaches

enthalten in: Journal of human genetics | 2014

von Lu, Y. | Zhou, X. | Jin, Z. | +10

5

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss

enthalten in: Genomics | 2014

von Du, W. | Cheng, J. | Ding, H. | +3

6

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

enthalten in: BMC genetics | 2014

von Zhu, Y. | Huang, S. | Kang, D. | +7

7

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

enthalten in: Journal of translational medicine | 2009

von Yuan, Y. | You, Y. | Huang, D. | +8

8

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss

enthalten in: Biochemical and biophysical research communications | 2007

von Yuan, H. | Chen, J. | Liu, X. | +11

9

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss

enthalten in: Biochemical and biophysical research communications | 2007

von Han, D. | Dai, P. | Zhu, Q. | +8

10

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

enthalten in: American journal of medical genetics. Part A | 2006

von Young, W. | Zhao, L. | Qian, Y. | +7