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Query Trace: Congenital Disorders of Glycosylation and TF[orginal query]

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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed