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Fengxia Yao

Showing results (31-40 of 34) with videos related to

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Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
European Journal of Human Genetics : EJHG|October 5, 2022
Identification and characterization of two DMD pedigrees with large inversion mutations based on a long-read sequencing pipelineChang Geng, Ciliu Zhang, Pidong Li, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic studyXiaoming Wei, Yi Dai, Ping Yu, et al.
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Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics|February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
European Journal of Human Genetics : EJHG|October 5, 2022
Identification and characterization of two DMD pedigrees with large inversion mutations based on a long-read sequencing pipelineChang Geng, Ciliu Zhang, Pidong Li, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic studyXiaoming Wei, Yi Dai, Ping Yu, et al.
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