Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia von Tsukada, Satoshi, Saffran, Douglas C., Rawlings, David J., Parolini, Ornella, Allen, R.Cutler, Klisak, Ivana, Sparkes, Robert S., Kubagawa, Hiromi, Mohandas, Thuluvancheri, Quan, Shirley, Belmont, John W., Cooper, Max D., Conley, Mary Ellen, Witte, Owen N.

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D2 dopamine receptor gene and cigarette smoking: A reward gene? von Noble, E.P., Jeor, S.T.St, Ritchie, T., Syndulko, K., Jeor, S.C.St, Fitch, R.J., Brunner, R.L., Sparkes, R.S.

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Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11 : linkage to convulsions and electroencephalography trait von LIU, A. W, DELGADO-ESCUETA, A. V, DONNADIEU, F. R, SPARKES, R. S, SERRATOSA, J. M, ALONSO, M. E, MEDINA, M. T, GEE, M. N, CORDOVA, S, ZHAO, H. Z, SPELLMAN, J. M, PEEK, J. R. R

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D2 and D4 dopamine receptor polymorphisms and personality von Noble, Ernest P., Ozkaragoz, Tulin Z., Ritchie, Terry L., Zhang, Xuxian, Belin, Thomas R., Sparkes, Robert S.

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The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships von Sweetser, D A, Birkenmeier, E H, Klisak, I J, Zollman, S, Sparkes, R S, Mohandas, T, Lusis, A J, Gordon, J I

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Assignment of the Human and Mouse Prion Protein Genes to Homologous Chromosomes von Sparkes, Robert S., Simon, Melvin, Cohn, Vivian H., Fournier, R. E. K., Lem, Janice, Klisak, Ivana, Heinzmann, Camilla, Blatt, Cila, Lucero, Michael, Mohandas, T., DeArmond, Stephen J., Westaway, David, Prusiner, Stanley B., Weiner, Leslie P.

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Reactivation of an Inactive Human X Chromosome: Evidence for X Inactivation by DNA Methylation von Mohandas, T., Sparkes, R. S., Shapiro, L. J.

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Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis von Ryan, Stephen G., Sherman, Stephanie L., Terry, Joseph C., Sparkes, Robert S., Torres, M. Cristina, Mackey, Ray W.

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Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy von Serratosa, José M., Delgado-Escueta, Antonio V., Medina, Marco T., Zhang, Quanwei, Iranmanesh, Reza, Sparkes, Robert S.

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Complementary homeo protein gradients in developing limb buds von OLIVER, G, SIDELL, N, FISKE, W, HEINZMANN, C, MOHANDAS, T, SPARKES, R. S, DE ROBERTIS, E. M

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A New Locus for Autosomal Dominant Cataract on Chromosome 12q13 von Bateman, J. Bronwyn, Johannes, Meriam, Flodman, Pamela, Geyer, David D, Clancy, Kevin P, Heinzmann, Camilla, Kojis, Tracy, Berry, Rebecca, Sparkes, Robert S, Spence, M. Anne

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Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa von KOJIS, T. L, HEINZMANN, C, FLODMAN, P, NGO, J. T, SPARKES, R. S, SPENCE, M. A, BATEMAN, J. B, HECKENLIVELY, J. R

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Lafora Progressive Myoclonus Epilepsy: Narrowing the Chromosome 6q24 Locus by Recombinations and Homozygosities von Sainz, Jesus, Minassian, Berge A., Serratosa, Jose M., Gee, Manyee N., Sakamoto, Lise M., Iranmanesh, Reza, Bohlega, Saeed, Baumann, Robert J., Ryan, Steve, Sparkes, Robert S., Delgado-Escueta, Antonio V.

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Genomic organization and chromosomal localization of a novel human hepatic dihydrodiol dehydrogenase with high affinity bile acid binding von HUAN LOU, HAMMOND, L, VISHVINDER SHARMA, SPARKES, R. S, LUSIS, A. J, STOLZ, A

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Linkage of an autosomal dominant clefting syndrome (Van der Woude) to Loci on chromosome Iq von MURRAY, J. C, NISHIMURA, D. Y, GLINSKI, L. P, PAULI, R. M, NAKAMURA, Y, GREEN, P. P, SCHINZEL, A, BUETOW, K. H, ARDINGER, H. H, SPENCE, M. A, SPARKES, R. S, FALK, R. E, FALK, P. M, GARDNER, R. J. M, HARKNESS, E. M

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Cloning of the human cholesterol 7 α-hydroxylase gene ( CYP7) and localization to chromosome 8q11–q12 von Cohen, Jonathan C., Cali, James J., Jelinek, Diane F., Mehrabian, Margarete, Sparkes, Robert S., Lusis, Aldons J., Russell, David W., Hobbs, Helen H.

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Molecular insights into Fanconi anemia von Sparkes, R S

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Regional Mapping of Human Chromosome 19: Organization of Genes for Plasma Lipid Transport (APOC1, -C2, and -E and LDLR) and the Genes C3, PEPD, and GPI von Lusis, A. J., Heinzmann, C., Sparkes, R. S., Scott, J., Knott, T. J., Geller, R., Sparkes, M. C., Mohandas, T.

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The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular... von Demmer, L.A., Birkenmeier, E.H., Sweetser, D.A., Levin, M.S., Zollman, S., Sparkes, R.S., Mohandas, T., Lusis, A.J., Gordon, J.I.

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Chromosomal localization of the human vesicular amine transporter genes von PETER, D, FINN, J. P, KLISAK, I, YONGJIAN LIU, KOJIS, T, HEINZMANN, C, ALI ROGHANI, SPARKES, R. S, EDWARDS, R. H

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