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2. French retrospective multicentric study of neonatal hemochromatosis: importance of autopsy and autoimmune maternal manifestations. Collardeau-Frachon S; Heissat S; Bouvier R; Fabre M; Baruteau J; Broue P; Cordier MP; Debray D; Debiec H; Ronco P; Guigonis V Pediatr Dev Pathol; 2012; 15(6):450-70. PubMed ID: 22901025 [TBL] [Abstract][Full Text] [Related]
3. Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism. Kelly AL; Lunt PW; Rodrigues F; Berry PJ; Flynn DM; McKiernan PJ; Kelly DA; Mieli-Vergani G; Cox TM J Med Genet; 2001 Sep; 38(9):599-610. PubMed ID: 11546828 [TBL] [Abstract][Full Text] [Related]
4. A case of neonatal hemochromatosis-like liver failure with spontaneous remission. Inui A; Fujisawa T; Kubo T; Sogo T; Komatsu H; Kagata Y J Pediatr Gastroenterol Nutr; 2005 Mar; 40(3):374-7. PubMed ID: 15735497 [No Abstract] [Full Text] [Related]
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