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Frontiers in Genetics|December 26, 2022
Opportunities and challenges for newborn screening and early diagnosis of rare diseases in Latin AmericaRoberto Giugliani, Silvia Castillo Taucher, Sylvia Hafez, et al.
Frontiers in Genetics|December 26, 2022
Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, ChinaSiyu Chang, Yi Yang, Feng Xu, et al.
Frontiers in Genetics|December 26, 2022
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effectsAlberto Brusati, Antonia Ratti, Viviana Pensato, et al.
Frontiers in Genetics|December 26, 2022
Review: Genetic and protein variants of milk caseins in goatsSiham A Rahmatalla, Danny Arends, Gudrun A Brockmann
Frontiers in Genetics|December 26, 2022
Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testingBeiping Zeng, Hongen Xu, Yanan Yu, et al.
Frontiers in Genetics|December 26, 2022
Differentially expressed gene profiles and associated ceRNA network in ATG7-Deficient lens epithelial cells under oxidative stressHongyu Li, Lixiong Gao, Jinlin Du, et al.
Frontiers in Genetics|December 26, 2022
Estimating genetic gains for tolerance to stress combinations in tropical maize hybridsAbebe Menkir, Ibnou Dieng, Silvestro Meseka, et al.
Frontiers in Genetics|December 26, 2022
A pan-cancer analysis of the prognostic value of long non-coding RNA LINC00662 in human cancersGuangming Zhang, Bin Wu, Liangyin Fu, et al.
Frontiers in Genetics|December 22, 2022
Corrigendum: m6A regulatory gene-mediated methylation modification in glioma survival predictionGuiyun Zhang, Ping Zheng, Yisong Lv, et al.
Frontiers in Genetics|December 22, 2022
Diagnostic signature, subtype classification, and immune infiltration of key m6A regulators in osteomyelitis patientsXiangwen Shi, Haonan Ni, Yipeng Wu, et al.
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