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Current Genomics
|
August 2, 2018
An <i>OTOF</i> Frameshift Variant Associated with Auditory Neuropathy Spectrum Disorder
Hong Xia, Xiangjun Huang, Hongbo Xu, et al.
Plos One
|
August 27, 2015
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
Hong Xia, Xiangjun Huang, Yi Guo, et al.
Biosensors & Bioelectronics
|
April 29, 2022
In-situ preparation of lactate-sensing membrane for the noninvasive and wearable analysis of sweat
Danfeng Jiang, Changshun Xu, Qingwen Zhang, et al.
Molecular Medicine Reports
|
January 24, 2017
Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1
Qian Lu, Lamei Yuan, Hongbo Xu, et al.
Journal of Cellular Biochemistry
|
January 19, 2019
A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey disease
Heng Xiao, Xiangjun Huang, Hongbo Xu, et al.
Bioscience Reports
|
February 14, 2018
Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome Sequencing
Xiangjun Huang, Lamei Yuan, Hongbo Xu, et al.
Biosensors & Bioelectronics
|
October 13, 2022
A miniaturized electrochemical device based on the nitrogen, carbon-codoped bimetal for real-time monitoring of acetaminophen and dopamine in urine
Danfeng Jiang, Xiangjun Huang, Qingwen Zhang, et al.
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Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
Current Genomics
|
August 2, 2018
An <i>OTOF</i> Frameshift Variant Associated with Auditory Neuropathy Spectrum Disorder
Hong Xia, Xiangjun Huang, Hongbo Xu, et al.
Plos One
|
August 27, 2015
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
Hong Xia, Xiangjun Huang, Yi Guo, et al.
Biosensors & Bioelectronics
|
April 29, 2022
In-situ preparation of lactate-sensing membrane for the noninvasive and wearable analysis of sweat
Danfeng Jiang, Changshun Xu, Qingwen Zhang, et al.
Molecular Medicine Reports
|
January 24, 2017
Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1
Qian Lu, Lamei Yuan, Hongbo Xu, et al.
Journal of Cellular Biochemistry
|
January 19, 2019
A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey disease
Heng Xiao, Xiangjun Huang, Hongbo Xu, et al.
Bioscience Reports
|
February 14, 2018
Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome Sequencing
Xiangjun Huang, Lamei Yuan, Hongbo Xu, et al.
Biosensors & Bioelectronics
|
October 13, 2022
A miniaturized electrochemical device based on the nitrogen, carbon-codoped bimetal for real-time monitoring of acetaminophen and dopamine in urine
Danfeng Jiang, Xiangjun Huang, Qingwen Zhang, et al.
Page
of 3