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Yin-Hung Lin

Showing results (1-10 of 24) with videos related to

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Biochemical and Biophysical Research Communications|August 3, 2007
A proteomic approach to study Salmonella enterica serovar Typhimurium putative transporter YjeH associated with ceftriaxone resistanceWensi S Hu, Yin-Hung Lin, Chun-Chieh Shih
Transfusion|May 18, 2018
ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepanciesPing Chun Wu, Yin-Hung Lin, Lei Fang Tsai, et al.
Mutation Research|March 17, 2015
Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencingYin-Hung Lin, Chen-Chi Wu, Tun-Yen Hsu, et al.
JAMA Otolaryngology-- Head & Neck Surgery|July 9, 2017
Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing LossPei-Hsuan Lin, Chuan-Jen Hsu, Yi-Hsin Lin, et al.
Plos One|March 2, 2013
Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairmentChen-Chi Wu, Yin-Hung Lin, Ying-Chang Lu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|September 13, 2020
Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermiaHuei-Ming Yeh, Min-Hua Liao, Chun-Lin Chu, et al.
Medicine|July 14, 2015
Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel SequencingChen-Chi Wu, Yin-Hung Lin, Tien-Chen Liu, et al.
Plos One|September 24, 2015
Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 MutationsChe-Ming Wu, Hui-Chen Ko, Yung-Ting Tsou, et al.
The Journal of Molecular Diagnostics : JMD|October 1, 2018
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular AqueductYin-Hung Lin, Chen-Chi Wu, Yi-Hsin Lin, et al.
The Laryngoscope|March 27, 2012
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndromeShih-Hao Wang, Chen-Chi Wu, Ying-Chang Lu, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

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Pageof 3
Biochemical and Biophysical Research Communications|August 3, 2007
A proteomic approach to study Salmonella enterica serovar Typhimurium putative transporter YjeH associated with ceftriaxone resistanceWensi S Hu, Yin-Hung Lin, Chun-Chieh Shih
Transfusion|May 18, 2018
ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepanciesPing Chun Wu, Yin-Hung Lin, Lei Fang Tsai, et al.
Mutation Research|March 17, 2015
Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencingYin-Hung Lin, Chen-Chi Wu, Tun-Yen Hsu, et al.
JAMA Otolaryngology-- Head & Neck Surgery|July 9, 2017
Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing LossPei-Hsuan Lin, Chuan-Jen Hsu, Yi-Hsin Lin, et al.
Plos One|March 2, 2013
Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairmentChen-Chi Wu, Yin-Hung Lin, Ying-Chang Lu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|September 13, 2020
Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermiaHuei-Ming Yeh, Min-Hua Liao, Chun-Lin Chu, et al.
Medicine|July 14, 2015
Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel SequencingChen-Chi Wu, Yin-Hung Lin, Tien-Chen Liu, et al.
Plos One|September 24, 2015
Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 MutationsChe-Ming Wu, Hui-Chen Ko, Yung-Ting Tsou, et al.
The Journal of Molecular Diagnostics : JMD|October 1, 2018
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular AqueductYin-Hung Lin, Chen-Chi Wu, Yi-Hsin Lin, et al.
The Laryngoscope|March 27, 2012
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndromeShih-Hao Wang, Chen-Chi Wu, Ying-Chang Lu, et al.
Pageof 3