Isolation, Characterization, and Precise Physical Localization of Human CDX1, a caudal-Type Homeobox Gene by Bonner, Cynthia A., Loftus, Stacie K., Wasmuth, John J.

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The Shaw-related potassium channel gene, Kv3.1, on human chromosome 11, encodes the type l K+ channel in T cells by Grissmer, S, Ghanshani, S, Dethlefs, B, McPherson, J D, Wasmuth, J J, Gutman, G A, Cahalan, M D, Chandy, K G

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Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel by PITTLER, S. J, LEE, A. K, ALTHERR, M. R, HOWARD, T. A, SELDIN, M. F, HURWITZ, R. L, WASMUTH, J. J, BAEHR, W

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Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers by CLERMONT, O, BURLET, P, LATHROP, M, MUNNICH, A, MELKI, J, BURGLEN, L, LEFEBVRE, S, PASCAL, F, MCPHERSON, J, WASMUTH, J. J, COHEN, D, LE PASLIER, D, WEISSENBACH, J

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Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q by RYAN, S. G, DIXON, M. J, NIGRO, M. A, KELTS, A, MARKAND, O. N, TERRY, J. C, SHIANG, R, WASMUTH, J. J, O'CONNELL, P

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Genomic Organization of the Human Heparan Sulfate-N-Deacetylase/N-Sulfotransferase Gene: Exclusion from a Causative Role in the Pathogenesis of Treacher Collins Syndrome by Gladwin, Amanda J., Dixon, Jill, Loftus, Stacie K., Wasmuth, John J., Dixon, Michael J.

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A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31. 3-32 by Dixon, J., Gladwin, A.J., Perveen, R., Dixon, M.J., Loftus, S.K., Wasmuth, J.J., Riley, J.H., Anand, R.

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Chromosome Jumping from D4S10 (G8) toward the Huntington Disease Gene by Richards, Julia E., Gilliam, T. Conrad, Cole, Jeffery L., Drumm, Mitchell L., Wasmuth, John J., Gusella, James F., Collins, Francis S.

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Cosmid probe CRI-C47 (D4S117) maps to 4p16.1 by WEIFFENBACH, B, ALTHERR, M, WASMUTH, J. J

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A highly polymorphic VNTR locus on the long arm of chromosome 4 by Altherr, M R, Wasmuth, J J, Nakamura, Y, White, R

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The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library by Snell, R.G., Doucette-Stamm, L.A., Gillespie, K.M., Taylor, S.A.M., Riba, L., Bates, G.P., Altherr, M.R., MacDonald, M.E., Gusella, J.F., Wasmuth, J.J., Lehrach, H., Housman, D.E., Harper, P.S., Shaw, D.J.

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Efficient procedure for transferring specific human genes into Chinese hamster cell mutants: interspecific transfer of the human genes encoding leucyl- and asparaginyl-tRNA synthet... by Cirullo, R E, Dana, S, Wasmuth, J J

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A highly polymorphic locus in 5p15.2-5p15.3 (213-274EC) revealed an anonymous single copy DNA fragment by OVERHAUSER, J, BEAUDET, A. L, WASMUTH, J. J

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Mbol RFLP at the D4S43 (C4H) locus by LAZAROU, L. P, SNELL, R. G, MACDONALD, M. E, GUSELLA, J. F, WASMUTH, J. J, SHAW, D. J

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MboI RFLP at the D4S43 (C4H) locus by Lazarou, L P, Snell, R G, MacDonald, M E, Gusella, J F, Wasmuth, J J, Shaw, D J

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Construction of a Not I linking library and isolation of new markers close to the Huntington's disease gene by Pohl, T.M., Zimmer, M., MacDonald, M.E., Smith, B., Bucan, M., Poustka, A., Volinia, S., Searle, S., Zehetner, G., Wasmuth, J.J., Gusella, J., Lehrach, H., Frischauf, A.-M.

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