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  • Title: Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
    Author: Gurrieri F, Cappa M, Neri G.
    Journal: Am J Med Genet; 1992 Sep 15; 44(2):136-7. PubMed ID: 1456280.
    Abstract:
    The Simpson-Golabi-Behmel syndrome is an X-linked condition characterized by pre- and postnatal overgrowth, "coarse" face, postaxial polydactyly, midline defects, and psychomotor development ranging from normal to mildly retarded. We report on an additional sporadic patient with novel manifestations, contributing to a more thorough delineation of this syndrome.
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