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Showing articles 0 to 10 of 10 Filter Applied: short stature (Click to remove) A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Mitochondrial Respiratory-Chain Diseases NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992 MELAS Syndrome Involving a Mother & Two Children Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987 Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients Lancet 2:85-91, Streissguth,A.P.,et al, 1985 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Kearns-Sayre Syndrome with Hypoparathyroidism Ann Neurol 3:513, Horwitz,S.J.,et al, 1978 Kearns-Sayre Syndrome & Hypoparathyroidism Ann Neurol 3:455, Pellock,J.M.,et al, 1978 Showing articles 0 to 10 of 10