Showing results 13 to 20 of 20
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Title | Author(s) | Issue Date | Views | |
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Megaconial Congenital Muscular Dystrophy: Same Novel Homozygous Mutation In Chkb Gene In Two Unrelated Chinese Patients Journal:Neuromuscular Disorders | 2020 | 46 | ||
Olfactory Dysfunction in Coronavirus Disease 2019 Patients: Observational Cohort Study and Systematic Review Journal:Open Forum Infectious Diseases | 2020 | 55 | ||
Organoid cultures reveal distinct genetic profile of early-onset colorectal cancer enriched for the serrated neoplasia pathway Proceeding/Conference:Cell Symposium: Engineering Organoids and Organs | 2019 | 25 | ||
2015 | ||||
2017 | 143 | |||
Treatment of Gastric Metaplasia or Dysplasia by Endoscopic Radiofrequency Ablation: A Pilot Study Journal:Hepato-Gastroenterology | 2015 | 69 | ||
Unraveling the oncogenic pathway of serrated polyposis syndrome driven by RNF43 germline mutation Proceeding/Conference:Cancer Research | 2017 | 83 | ||
X-linked Dilated Cardiomyopathy with mutation In The 5′ Splice Site Intron 1 Of Dystrophin Gene With Utrophin Upregulation Journal:Journal of Pediatric Neurology | 2018 |