受强制性开放获取政策约束的文章 - Amal Bouzid了解详情
无法在其他位置公开访问的文章：1 篇
SRD5A3‐CDG: 3D structure modeling, clinical spectrum, and computer‐based dysmorphic facial recognition
I Ben Ayed, W Ouarda, F Frikha, F Kammoun, A Souissi, M Ben Said, ...
American Journal of Medical Genetics Part A 185 (4), 1081-1090, 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：10 篇
The evolving SARS-CoV-2 epidemic in Africa: Insights from rapidly expanding genomic surveillance
H Tegally, JE San, M Cotten, M Moir, B Tegomoh, G Mboowa, DP Martin, ...
Science 378 (6615), eabq5358, 2022
强制性开放获取政策： Bill & Melinda Gates Foundation, US Department of Defense, US National …
CDC14A phosphatase is essential for hearing and male fertility in mouse and human
A Imtiaz, IA Belyantseva, AJ Beirl, C Fenollar-Ferrer, R Bashir, I Bukhari, ...
Human molecular genetics 27 (5), 780-798, 2018
强制性开放获取政策： US National Institutes of Health
Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population
A Souissi, MB Said, IB Ayed, I Elloumi, A Bouzid, MA Mosrati, M Hasnaoui, ...
Journal of Advanced Research 31, 13-24, 2021
强制性开放获取政策： European Commission
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing
A Yahia, IB Ayed, AA Hamed, IN Mohammed, MA Elseed, AM Bakhiet, ...
Annals of Human Genetics 86 (4), 181-194, 2022
强制性开放获取政策： European Commission
Evaluation of the Genetic Association and mRNA Expression of the COL1A1, BMP2, and BMP4 Genes in the Development of Otosclerosis
K Hansdah, N Singh, A Bouzid, S Priyadarshi, CS Ray, A Desai, ...
Genetic Testing and Molecular Biomarkers 24 (6), 343-351, 2020
强制性开放获取政策： Department of Science & Technology, India
Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritis
HR Gouda, IM Talaat, A Bouzid, H El-Assi, A Nabil, T Venkatachalam, ...
Frontiers in immunology 13, 960068, 2022
强制性开放获取政策： German Research Foundation
The risks of RELN polymorphisms and its expression in the development of otosclerosis
S Priyadarshi, K Hansdah, N Singh, A Bouzid, CS Ray, KC Panda, ...
Plos one 17 (6), e0269558, 2022
强制性开放获取政策： Department of Science & Technology, India
Genetic variants and altered expression of SERPINF1 confer disease susceptibility in patients with otosclerosis
N Singh, K Hansdah, A Bouzid, CS Ray, A Desai, KC Panda, ...
Journal of Human Genetics 68 (9), 635-642, 2023
强制性开放获取政策： Department of Science & Technology, India
Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region
I Ben Ayed, O Jallouli, Y Murakami, A Souissi, S Mallouli, A Bouzid, ...
Frontiers in Neurology 14, 1092887, 2023
强制性开放获取政策： European Commission
Gene duplication and functional divergence of the zebrafish otospiralin genes
A Baanannou, S Rastegar, A Bouzid, M Takamiya, V Gerber, A Souissi, ...
Development Genes and Evolution 230, 27-36, 2020
强制性开放获取政策： Federal Ministry of Education and Research, Germany
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