Molecular Cloning, cDNA Structure, and Chromosomal Localization of the Human Type II cGMP-Dependent Protein Kinase von Ørstavik, S, Solberg, R, Taskén, K, Nordahl, M, Altherr, M.R, Hansson, V, Jahnsen, T, Sandberg, M

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Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events von Weiffenbach, B, Dubois, J, Storvick, D, Tawil, R, Jacobsen, S.J, Gilbert, J, Wijmenga, C, Mendell, J.R, Winokur, S, Altherr, M.R, Schultz, P, Olandt, S, Frants, R.R, Pericak-Vance, M, Griggs, R.C

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Genomic organization of the human fibroblast growth factor receptor 3 (FGFR3) gene and comparative sequence analysis with the mouse Fgfr3 gene von PEREZ-CASTRO, A. V, WILSON, J, ALTHERR, M. R

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Genomics of the Bacillus cereus group of organisms von Rasko, D.A, Altherr, M.R, Han, C.S, Ravel, J

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Assignment of SOD3 to human chromosome band 4p15.3→p15.1 with somatic cell and radiation hybrid mapping, linkage mapping, and fluorescent in-situ hybridization von Stern, L.F., Chapman, N.H., Wijsman, E.M., Altherr, M.R., Rosen, D.R.

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Genomic Organization of the Mouse Fibroblast Growth Factor Receptor 3 (Fgfr3) Gene von Perez-Castro, Ana V., Wilson, Julie, Altherr, Michael R.

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Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel von PITTLER, SJ, LEE, AK, ALTHERR, MR, HOWARD, TA, SELDIN, MF, HURWITZ, RL, WASMUTH, JJ, BAEHR, W

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A YAC Contig Spanning a Cluster of Human Type III Receptor Protein Tyrosine Kinase Genes (PDGFRA-KIT-KDR) in Chromosome Segment 4q12 von Spritz, R.A., Strunk, K.M., Lee, S.-T., Lu-Kuo, J.M., Ward, D.C., Le Paslier, D., Altherr, M.R., Dorman, T.E., Moir, D.T.

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Genetic and physical maps of human chromosome 4 based on dinucleotide repeats von Mills, K.A., Buetow, K.H., Xu, Y., Weber, J.L., Altherr, M.R., Wasmuth, J.J., Murray, J.C.

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A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD) von WINOKUR, S. T, SCHUTTE, B, WEIFFENBACH, B, WASHINGTON, S. S, MCELLIGOTT, D, ARAVINDA CHAKRAVARTI, WASMUTH, J. H, ALTHERR, M. R

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"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype von Zollino, M., Wright, T.J., Di Stefano, C., Tosolini, A., Battaglia, A., Altherr, M.R., Neri, G.

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Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13. 1-q21. 1 and mouse chromosome 5 von Kaiser, U.B., Dushkin, H., Beier, D.R., Chin, W.W., Altherr, M.R.

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Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus von Haraguchi, Y., Chung, A.B., Torroni, A., Stepien, G., Shoffner, J.M., Wasmuth, J.J., Costigan, D.A., Polak, M., Altherr, M.R., Winokur, S.T., Wallace, D.C.

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Radiation hybrid map spanning the huntington disease gene region of chromosome 4 von Altherr, M.R., Plummer, S., Bates, G., MacDonald, M., Taylor, S., Lehrach, H., Frischauf, A.-M., Gusella, J.F., Boehnke, M., Wasmuth, J.J.

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A highly polymorphic VNTR locus on the long arm of chromosome 4 von 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 von 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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YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene von Weiffenbach, B., Dubois, J., Manning, S., Ma, N.S., Schutte, B.C., Winokur, S.T., Altherr, M.R., Jacobsen, S.J., Stanton, V.P., Yokoyama, Kazushige, Moir, D.

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FISH detection of Wolf-Hirschhorn syndrome : exclusion of D4F26 as critical site von JOHNSON, V. P, ALTHERR, M. R, BLAKE, J. M, KEPPEN, L. D

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