Enter your terms above and click the 'Search' button.

Showing articles 0 to 12 of 12 Filter Applied: mucopolysaccharidoses (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease (Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983 Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Corneal Opacification in Infancy MCV Quart 8:230, Ching,F., 1972 Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue (Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972 The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults Neurol 41:794-798, Coker,S.B., 1991 Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl Clin genet 37:355-362, Clarke,J.T.,et al, 1990 Clinicopathological Conference Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983 Infantile Metachromatic Leukodystrophy NEJM 288:1365, 14051973., Leroy,J.,et al, 1973 The Mucopolysaccharidoses (Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith W. B. , Saunders Co. , 1970, 248-249., David,W., 1970 Showing articles 0 to 12 of 12