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Guang Tang

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Human Genetics|March 17, 2004

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24Bei-Sha Tang, Wei Luo, Kun Xia, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample StudyWo-Tu Tian, Fei-Xia Zhan, Zhen-Hua Liu, et al.

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Search research articles

Showing results (101-110 of 103) with videos related to

Sort By:

Pageof 11

You have reached the last page of results.This site can display upto 103 results.

Human Genetics|March 17, 2004

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24Bei-Sha Tang, Wei Luo, Kun Xia, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample StudyWo-Tu Tian, Fei-Xia Zhan, Zhen-Hua Liu, et al.

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