受强制性开放获取政策约束的文章 - Mohammad-Sadegh Fallah了解详情
无法在其他位置公开访问的文章：2 篇
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
Nat Genet 46 (3), 294-8, 2014
强制性开放获取政策： Danish Council for Independent Research
Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS)
LNH Bonab, M Moazzam-Jazi, RSM Moosavi, MS Fallah, H Lanjanian, ...
Gene 778, 145485, 2021
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：3 篇
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia
ZY Yap, S Efthymiou, S Seiffert, KV Parra, S Lee, A Nasca, R Maroofian, ...
The American Journal of Human Genetics 108 (12), 2368-2384, 2021
强制性开放获取政策： US National Institutes of Health, German Research Foundation, Netherlands …
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
DL Polla, MA Farazi Fard, Z Tabatabaei, P Habibzadeh, OA Levchenko, ...
Genetics in medicine 23 (7), 1246-1254, 2021
强制性开放获取政策： US National Institutes of Health, European Commission
Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta
TT Tran, RB Keller, B Guillemyn, M Pepin, JE Corteville, S Khatib, ...
Human Genetics and Genomics Advances 2 (4), 2021
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
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