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7. Transferrin microheterogeneity as a probe in normal and disease states. De Jong G; Feelders R; Van Noort WL; Van Eijk HG Glycoconj J; 1995 Jun; 12(3):219-26. PubMed ID: 7496135 [TBL] [Abstract][Full Text] [Related]
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14. Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type I. Mayatepek E; Schröder M; Kohlmüller D; Bieger WP; Nützenadel W Acta Paediatr; 1997 Oct; 86(10):1138-40. PubMed ID: 9350901 [TBL] [Abstract][Full Text] [Related]
15. A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity. Charlwood J; Clayton P; Johnson A; Keir G; Mian N; Winchester B J Inherit Metab Dis; 1997 Nov; 20(6):817-26. PubMed ID: 9427152 [TBL] [Abstract][Full Text] [Related]
16. Transferrin variants: pitfalls in the diagnostics of Congenital disorders of glycosylation. Zühlsdorf A; Park JH; Wada Y; Rust S; Reunert J; DuChesne I; Grüneberg M; Marquardt T Clin Biochem; 2015 Jan; 48(1-2):11-3. PubMed ID: 25305627 [TBL] [Abstract][Full Text] [Related]
17. Prenatal hypertrophic cardiomyopathy and pericardial effusion in carbohydrate-deficient glycoprotein syndrome. García Silva MT; de Castro J; Stibler H; Simón R; Chasco Yrigoyen A; Mateos F; Ferrer I; Madero S; Velasco JM; Guttierrez-Larraya F J Inherit Metab Dis; 1996; 19(2):257-9. PubMed ID: 8739980 [No Abstract] [Full Text] [Related]
18. Carbohydrate-deficient glycoprotein syndromes: inborn errors of protein glycosylation. Keir G; Winchester BG; Clayton P Ann Clin Biochem; 1999 Jan; 36 ( Pt 1)():20-36. PubMed ID: 10370757 [TBL] [Abstract][Full Text] [Related]
19. Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicism. Knopf C; Rod R; Jaeken J; Berant M; Van Schaftingen E; Fryns JP; Brill-Zamir R; Gershoni-Baruch R; Lischinsky S; Mandel H J Inherit Metab Dis; 2000 Jun; 23(4):399-403. PubMed ID: 10896304 [No Abstract] [Full Text] [Related]