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Showing articles 0 to 10 of 10 Filter Applied: dysmorphic (Click to remove) Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Angelman Syndrome Revisited Neurologist 13:305-312, Paprocka,J.,et al, 2007 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium Neurol 100:631-637, Zeng,T.f.,et al, 2023 MR Brain Imaging of Fucosidosis Type I AJNR 22:777-780, Galluzzi,P.,et al, 2001 The Exercise Test in Andersen Syndrome Arch Neurol 56:352-356, Katz,J.S.,et al, 1999 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 Showing articles 0 to 10 of 10