HuGE Literature Finder
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Records 1-3
Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.
Pediatric research 2018 01 83 (1-1): 119-127. de la Morena-Barrio María E, Ballesta-Martínez María J, López-Gálvez Raquel, Antón Ana I, López-González Vanessa, Martínez-Ribot Laia, Padilla José, Miñano Antonia, García-Algar Oscar, Del Campo Miguel, Corral Javier, Guillén-Navarro Encarna, Vicente Vicen |
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation.
Journal of neurology 2015 Jan 262 (1): 154-64. Barone Rita, Carrozzi M, Parini R, Battini R, Martinelli D, Elia M, Spada M, Lilliu F, Ciana G, Burlina A, Leuzzi V, Leoni M, Sturiale L, Matthijs G, Jaeken J, Di Rocco M, Garozzo D, Fiumara |
Genetic variants of transferrin in cystic fibrosis.
Journal of inherited metabolic disease 2008 Jun 31 (3): 457-61. Marklová E, Albahri Z, Vanícek H, Dedek P, Valis M, Kopácová M, Vávrová |
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- Page last updated:Dec 12, 2019
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