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44. A new genetic fibrinogen variant (fibrinogen Erfurt I). Structurally characterized by an abnormal B beta-chain and present both in plasma and platelets. Meyer M; Schellenberg I; Vogel G; Bischoff I Thromb Haemost; 1988 Apr; 59(2):138-42. PubMed ID: 3388290 [TBL] [Abstract][Full Text] [Related]
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47. Fibrinogen Irvine: a qualitatively abnormal fibrinogen associated with the predisposition to recurrent visceral and peripheral venous thrombosis. Lehmer RR; Elias AN; Capdeville MJ; Brown DR; Branson HE J Natl Med Assoc; 1985 Jul; 77(7):561-5. PubMed ID: 4046054 [TBL] [Abstract][Full Text] [Related]
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54. Congenital nephrotic syndrome of Finnish type and other types of early familial nephrotic syndromes. Norio R Birth Defects Orig Artic Ser; 1974; 10(4):69-72. PubMed ID: 4470912 [TBL] [Abstract][Full Text] [Related]
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56. The familial nephrotic syndrome. II. A clinicopathological study. Moncrieff MW; White RH; Glasgow EF; Winterborn MH; Cameron JS; Ogg CS Clin Nephrol; 1973; 1(4):220-9. PubMed ID: 4206018 [No Abstract] [Full Text] [Related]
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59. Cryofibrinogenemia: report of a case. Bair JS; Wu YC; Lü YC J Formos Med Assoc; 1991 Jan; 90(1):99-104. PubMed ID: 1679117 [TBL] [Abstract][Full Text] [Related]
60. Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome. Garty BZ; Eisenstein B; Sandbank J; Kaffe S; Dagan R; Gadoth N J Med Genet; 1994 Feb; 31(2):121-5. PubMed ID: 8182716 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]