History of Human Parasitology von COX, F. E. G

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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders von Miller, D T, Shen, Y, Weiss, L A, Korn, J, Anselm, I, Bridgemohan, C, Cox, G F, Dickinson, H, Gentile, J, Harris, D J, Hegde, V, Hundley, R, Khwaja, O, Kothare, S, Luedke, C, Nasir, R, Poduri, A, Prasad, K, Raffalli, P, Reinhard, A, Smith, S E, Sobeih, M M, Soul, J S, Stoler, J, Takeoka, M, Tan, W-H, Thakuria, J, Wolff, R, Yusupov, R, Gusella, J F, Daly, M J, Wu, B-L

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Concomitant infections, parasites and immune responses von COX, F. E. G.

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Analysis of upstream glucokinase promoter activity in transgenic mice and identification of glucokinase in rare neuroendocrine cells in the brain and gut von JETTON, T. L, YIN LIANG, PETTEPHER, C. C, ZIMMERMAN, E. C, COX, F. G, HORVATH, K, MATSCHINSKY, F. M, MAGNUSON, M. A

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P822: A PHASE 1 SINGLE ASCENDING DOSE STUDY OF CAN106, A LONG‐ACTING ANTI‐C5 COMPLEMENT MONOCLONAL ANTIBODY IN CLINICAL DEVELOPMENT FOR PNH AND OTHER COMPLEMENT‐MEDIATED DISEASES... von KHOO, C. M., SONG, X., WU, Q., COX, G. F.

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George Henry Falkiner Nuttall and the origins of parasitology and Parasitology von COX, F. E. G.

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Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome von Johnston, Jennifer, Kelley, Richard I., Feigenbaum, Annette, Cox, Gerald F., Iyer, Geeta S., Funanage, Vicky L., Proujansky, Roy

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Design and implementation of the North American Pediatric Cardiomyopathy Registry von Grenier, Michelle A, Osganian, Stavroula K, Cox, Gerald F, Towbin, Jeffrey A, Colan, Steven D, Lurie, Paul R, Sleeper, Lynn A, Orav, E.John, Lipshultz, Steven E

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Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency von Cox, Gerald F., Souri, Masayoshi, Aoyama, Toshifumi, Rockenmacher, Sol, Varvogli, Liza, Rohr, Frances, Hashimoto, Takashi, Korson, Mark S.

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Successful pregnancy and breastfeeding in a woman with mucopolysaccharidosis type I while receiving laronidase enzyme replacement. therapy von Castorina, M, Antuzzi, D, Richards, S M, Cox, G F, Xue, Y

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20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits von Lalani, S R, Thakuria, J V, Cox, G F, Wang, X, Bi, W, Bray, M S, Shaw, C, Cheung, S W, Chinault, A C, Boggs, B A, Ou, Z, Brundage, E K, Lupski, J R, Gentile, J, Waisbren, S, Pursley, A, Ma, L, Khajavi, M, Zapata, G, Friedman, R, Kim, J J, Towbin, J A, Stankiewicz, P, Schnittger, S, Hansmann, I, Ai, T, Sood, S, Wehrens, X H, Martin, J F, Belmont, J W, Potocki, L

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Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome von Mykytyn, Kirk, Nishimura, Darryl Y., Searby, Charles C., Shastri, Mythreyi, Yen, Hsan-jan, Beck, John S., Braun, Terry, Streb, Luan M., Cornier, Alberto S., Cox, Gerald F., Fulton, Anne B., Carmi, Rivka, Lüleci, Güven, Chandrasekharappa, Settara C., Collins, Francis S., Jacobson, Samuel G., Heckenlively, John R., Weleber, Richard G., Stone, Edwin M., Sheffield, Val C.

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Clinical approach to genetic cardiomyopathy in children von SCHWARTZ, M. L, COX, G. F, LIN, A. E, KORSON, M. S, PEREZ-ATAYDE, A, LACRO, R. V, LIPSHULTZ, S. E

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Mitochondrial neurogastrointestinal encephalomyopathy : Diagnosis by rectal biopsy von PEREZ-ATAYDE, A. R, FOX, V, TEITELBAUM, J. E, ANTHONY, D. A, FADIC, R, KALSNER, L, RIVKIN, M, JOHNS, D. R, COX, G. F

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Evaluation of Complex Inheritance Involving the Most Common Bardet-Biedl Syndrome Locus ( BBS1) von Mykytyn, Kirk, Nishimura, Darryl Y., Searby, Charles C., Beck, Gretel, Bugge, Kevin, Haines, Heidi L., Cornier, Alberto S., Cox, Gerald F., Fulton, Anne B., Carmi, Rivka, Iannaccone, Alessandro, Jacobson, Samuel G., Weleber, Richard G., Wright, Alan F., Riise, Ruth, Raoul Hennekam, C.M., Lüleci, Güven, Berker-Karauzum, Sibel, Biesecker, Leslie G., Stone, Edwin M., Sheffield, Val C.

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Dystrophies and heart disease von Cox, Gerald F, Kunkel, Louis M

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A Mutation in the Alpha 3 Chain of type IX Collagen Causes Autosomal Dominant Multiple Epiphyseal Dysplasia with Mild Myopathy von Bonnemann, Carsten G., Cox, Gerald F., Shapiro, Frederic, Wu, Jiann-Jiu, Feener, Chris A., Thompson, Teryl G., Anthony, Douglas C., Eyre, David R., Darras, Basil T., Kunkel, Louis M.

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A muscle-specific DNase I-like gene in human Xq28 von Parrish, Julia E., Ciccodicola, Alfredo, Wehnert, Manfred, Cox, Gerald F., Chen, Ellson, Nelson, David L.

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Equations for Determining the Gas and Brine Volumes in Sea-Ice Samples von Cox, G. F. N., Weeks, W. F.

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Incidence, Causes, and Outcomes of Dilated Cardiomyopathy in Children von Towbin, Jeffrey A, Lowe, April M, Colan, Steven D, Sleeper, Lynn A, Orav, E. John, Clunie, Sarah, Messere, Jane, Cox, Gerald F, Lurie, Paul R, Hsu, Daphne, Canter, Charles, Wilkinson, James D, Lipshultz, Steven E

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