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  • Title: Coffin-Lowry syndrome: a multicenter study.
    Author: Gilgenkrantz S, Mujica P, Gruet P, Tridon P, Schweitzer F, Nivelon-Chevallier A, Nivelon JL, Couillault G, David A, Verloes A.
    Journal: Clin Genet; 1988 Oct; 34(4):230-45. PubMed ID: 3069251.
    Abstract:
    The Coffin-Lowry syndrome is an inherited syndrome of mental retardation, characteristic facies and skeletal anomalies. The occurrence of severe manifestations in males, with no instance of male-to-male transmission, suggests an X-linked inheritance. The paper describes seven families from five European Centers.
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