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Results: 1-4 |
Results: 4

Authors: Schwartz, Charles E. May, Melanie M. Carpenter, Nancy J. Rogers, CUris R. Martin, Judith Bialer, Martin G. Ward, Jewell Sananbria, Javier Marsa, Silvana Lewis, James A. Echeverri, Roberto Lubs, Herbert A. Voeller, Kytja Simensen, Richard J. Stevenson, Roger E.
Citation: E. Schwartz, Charles et al., Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene, American journal of human genetics , 77(1), 2005, pp. 41-53

Authors: Stevenson, Roger E. Goodman, Harold O. Schwartz, Charles E. Simensen, Richard J. McLean, William T. Jr Herndon, C. Nash
Citation: E. Stevenson, Roger et al., Allan-Herndon syndrome. I. Clinical studies., American journal of human genetics , 47-I(3), 1990, pp. 446-453

Authors: Schwartz, Charles E. Ulmer, Joan Brown, Angela Pancoast, Ian Goodman, Harold O. Stevenson, Roger E.
Citation: E. Schwartz, Charles et al., Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21., American journal of human genetics , 47-I(3), 1990, pp. 454-458

Authors: Schwartz, Charles E. Johnson, John P. Holycross,Bridget Mandeville, Tracy M. Sears, Tena S. Graul, Elizabeth A. Carey, John C. Schroer, Richard J. Phelan, Mary C. Szollar, Judith Flannery, David B. Stevenson, Roger E.
Citation: E. Schwartz, Charles et al., Detection of submicroscopic deletions in band 17p13 in patients with the miller-dieker syndrome, American journal of human genetics , 43-II(5), 1988, pp. 597-604
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