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Genetics in Medicine : Official Journal of the American College of Medical Genetics
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February 27, 2022
MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variants
Fang Shen, Yongjia Yang, Yu Zheng, et al.
Molecular Genetics & Genomic Medicine
|
December 25, 2021
A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis
Fang Shen, Yongjia Yang, Pengcheng Li, et al.
Annals of Translational Medicine
|
August 25, 2021
Cost-effectiveness analysis of hemodialysis plus hemoperfusion versus hemodialysis alone in adult patients with end-stage renal disease in China
Haiyin Wang, Huajie Jin, Wendi Cheng, et al.
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of 2
Search research articles
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Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 27, 2022
MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variants
Fang Shen, Yongjia Yang, Yu Zheng, et al.
Molecular Genetics & Genomic Medicine
|
December 25, 2021
A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis
Fang Shen, Yongjia Yang, Pengcheng Li, et al.
Annals of Translational Medicine
|
August 25, 2021
Cost-effectiveness analysis of hemodialysis plus hemoperfusion versus hemodialysis alone in adult patients with end-stage renal disease in China
Haiyin Wang, Huajie Jin, Wendi Cheng, et al.
Page
of 2