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Showing articles 0 to 2 of 2 Filter Applied: short stature (Click to remove) Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy Neurol 57:1963-1968, Jeannet,P.,et al, 2001 Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence (Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975 Showing articles 0 to 2 of 2