Suchergebnisse - "YUAN HUIJUN"

PubPharm (7)

1

Quantitative thresholds for variant enrichment in 13,845 cases : improving pathogenicity classification in genetic hearing loss

enthalten in: Genome medicine | 2023

von Liu, S. | Zhong, M. | Huang, Y. | +11

2

Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss

enthalten in: Genome medicine | 2023

von Liu, S. | Zhong, M. | Huang, Y. | +11

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

Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family

enthalten in: Annals of human genetics | 2014

von Cheng, J. | Zhou, X. | Lu, Y. | +10

5

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

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

Mutation of the ATP-gated P2X₂ receptor leads to progressive hearing loss and increased susceptibility to noise

Erschienen: 2013

von Yan, D. | Zhu, Y. | Walsh, T. | +19

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