Suchergebnisse - "YUAN HUIJUN"

PubPharm (9)

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

Application of SNPscan in Genetic Screening for Common Hearing Loss Genes

enthalten in: PloS one | 2016

von Gao, Z. | Lu, Y. | Ke, J. | +10

3

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

4

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

5

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

6

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss

enthalten in: Physiological genomics | 2009

von Dai, P. | Stewart, A. | Chebib, F. | +19

ErratumIn: Physiol Genomics. 2010 Feb;40(3):216

7

Molecular etiology of hearing impairment in Inner Mongolia : mutations in SLC26A4 gene and relevant phenotype analysis

enthalten in: Journal of translational medicine | 2008

von Dai, P. | Yuan, Y. | Huang, D. | +7

8

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2008

von Dai, P. | Li, Q. | Huang, D. | +13

9

Genotypic analysis of familial dilated vestibular aqueduct syndrome

enthalten in: Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology | 2006

von Dai, P. | Han, D. | Cao, J. | +10

1
[1]