Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and EIF2B4[original query] |
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| Hyperinsulinaemic hypoglycaemia: A rare association of vanishing white matter disease. JIMD reports 2020 2 51 (1): 11-16. Bursle Carolyn, Yiu Eppie M, Yeung Alison, Freeman Jeremy L, Stutterd Chloe, Leventer Richard J, Vanderver Adeline, Yaplito-Lee J |
| Genotypic and phenotypic heterogeneity among Chinese pediatric genetic white matter disorders. Italian journal of pediatrics 2023 11 49 (1): 155. Liling Dong, Li Shang, Caiyan Liu, Chenhui Mao, Xinying Huang, Shanshan Chu, Bin Peng, Liying Cui, Jing G |
| Ovarioleukodystrophy Due to EIF2B Genes: Systematic Review and Case Report. Cureus 2024 8 16 (7): e64497. Mariana Escobar-Pacheco, Mariana Luna-Álvarez, David Dávila-Ortiz de Montellano, Petra Yescas-Gómez, Miguel Á Ramírez-Garc |
| Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing. BMC medical genomics 2024 4 17 (1): 98. Anett Illés, Henriett Pikó, Kristóf Árvai, Veronika Donka, Olívia Szepesi, János Kósa, Péter Lakatos, Artúr Be |
- Page last reviewed:Feb 1, 2024
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