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24. ECEL1 mutation causes fetal arthrogryposis multiplex congenita. Dohrn N; Le VQ; Petersen A; Skovbo P; Pedersen IS; Ernst A; Krarup H; Petersen MB Am J Med Genet A; 2015 Apr; 167A(4):731-43. PubMed ID: 25708584 [TBL] [Abstract][Full Text] [Related]
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39. Arthrogryposis multiplex congenita with posterior column degeneration and peripheral neuropathy: a case report. Folkerth RD; Guttentag SH; Kupsky WJ; Kinney HC Clin Neuropathol; 1993; 12(1):25-33. PubMed ID: 8382571 [TBL] [Abstract][Full Text] [Related]
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