“Invitation to Learning” Discusses A History of Western Philosophy von Edman, Irwin, Kallen, Horace M, Taylor, Harold A, Spencer, Lukas

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A Case of Progressive Quadriceps Weakness and Elevated Creatine Kinase Level Mimicking Inclusion Body Myositis von Leung, Doris G., Taylor, Harold A., Lindy, Amanda S., Basehore, Monica J., Mammen, Andrew L.

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Molecular order in mucolipidosis II and III nomenclature von Cathey, Sara S., Kudo, Mariko, Tiede, Stephan, Raas-Rothschild, Annick, Braulke, Thomas, Beck, Michael, Taylor, Harold A., Canfield, William M., Leroy, Jules G., Neufeld, Elizabeth F., McKusick, Victor A.

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X-Linked Mental Retardation with Seizures and Carrier Manifestations Is Caused by a Mutation in the Creatine-Transporter Gene (SLC6A8) Located in Xq28 von Hahn, Kimberly A., Salomons, Gajja S., Tackels-Horne, Darci, Wood, Tim C., Taylor, Harold A., Schroer, Richard J., Lubs, Herbert A., Jakobs, Cornelis, Olson, Rick L., Holden, Kenton R., Stevenson, Roger E., Schwartz, Charles E.

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“Invitation to Learning” Discusses A History of Western Philosophy von Edman, Irwin, Kallen, Horace M., Taylor, Harold A., Spencer, Lukas

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Response to Feingold's: The use of inappropriate, demeaning, and perjorative terminology to describe syndromes von Saul, Robert A., Taylor, Harold A., Leroy, Jules, Spranger, Jurgen, Proud, Virginia

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On sunset highways; a book of motor rambles in California von Murphy, Thomas Dowler, 1866

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β-Galactosidase Gene Mutations in Patients With Slowly Progressive GM1 Gangliosidosis von Kaye, Edward M., Shalish, Christo, Livermore, James, Taylor, Harold A., Stevenson, Roger E., Breakefield, Xandra O.

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Mucolipidosis III (Pseudo-Hurler Polydystrophy): Multiple Lysosomal Enzyme Abnormalities in Serum and Cultured Fibroblast Cells von Thomas, George H, Taylor, Harold A, Reynolds, Linda W, Miller, Carol S

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Genetic complementation after fusion of Tay-Sachs and Sandhoff cells von THOMAS, GEORGE H, TAYLOR, HAROLD A, MILLER, CAROL S, AXELMAN, JOYCE, MIGEON, BARBARA R

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Hazards of Oral Anticoagulants during Pregnancy von Stevenson, Roger E, Burton, O Marion, Ferlauto, Gerald J, Taylor, Harold A

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The Genteel Tradition in Liberal Education von Taylor, Harold A.

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Clinical, pathological, and biochemical studies on an infantile case of sulfatide/GM1 activator protein deficiency von Wenger, David A., DeGala, Gregory, Williams, Carolyn, Taylor, Harold A., Stevenson, Roger E., Pruitt, James R., Miller, John, Garen, Paul D., Balentine, J. Douglas

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b-Galactosidase Gene Mutations in Patients With Slowly Progressive GM1 Gangliosidosis von Kaye, Edward M, Shalish, Christo, Livermore, James, Taylor, Harold A, Stevenson, Roger E, Breakefield, Xandra O

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Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile type von Stevenson, R E, Lubinsky, M, Taylor, H A, Wenger, D A, Schroer, R J, Olmstead, P M

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Prenatal mucolipidosis type II (I-cell disease) can present as Pacman dysplasia von Saul, Robert A., Proud, Virginia, Taylor, Harold A., Leroy, Jules G., Spranger, Jurgen

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Cutis gyratum and acanthosis nigricans associated with other anomalies: A distinctive syndrome von Stevenson, Roger E., Ferlauto, Gerald J., Taylor, Harold A.

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Mannosidosis: Deficiency of a specific α-mannosidase component in cultured fibroblasts von Taylor, Harold A., Thomas, George H., Aylsworth, Arthur, Stevenson, Roger E., Reynolds, Linda W.

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Future granite production of Spain and India in 2014 von Taylor, Jr., Harold A

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Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion von Phelan, Mary C., Thomas, Gordon R., Saul, Robert A., Rogers, R. Curtis, Taylor, Harold A., Wenger, David A., McDermid, Heather E.

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