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Filter Applied: familial (Click to remove)

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992



Showing articles 0 to 3 of 3