Search Results - Leysens, Nancy

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  1. 1
    Linkage of Inflammatory Bowel Disease to Human Chromosome 6p

    Linkage of Inflammatory Bowel Disease to Human Chromosome 6p by Hampe, Jochen, Shaw, Sarah H., Saiz, Robert, Leysens, Nancy, Lantermann, Annette, Mascheretti, Silvia, Lynch, Nicholas J., MacPherson, Andrew J.S., Bridger, Stephen, van Deventer, Sander, Stokkers, Pieter, Morin, Phil, Mirza, Mudassar M., Forbes, Alastair, Lennard-Jones, John E., Mathew, Christopher G., Curran, Mark E., Schreiber, Stefan

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  2. 2
    Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans

    Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans by Lidral, Andrew C., Romitti, Paul A., Basart, Ann M., Doetschman, Thomas, Leysens, Nancy J., Daack-Hirsch, Sandra, Semina, Elena V., Johnson, Lisa R., Machida, Junichiro, Burds, Aurora, Parnell, Timothy J., Rubenstein, John L.R., Murray, Jeffrey C.

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  3. 3
    Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus

    Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus by Peiffer-Schneider, S, Schutte, B C, Murray, J C, Frees, K L, Williamson, K, Leysens, N J, Schwartz, D A

    Published in Mammalian genome
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  4. 4
    Cloning, Characterization, and Mapping of the Mouse Homeobox GeneHmx1

    Cloning, Characterization, and Mapping of the Mouse Homeobox GeneHmx1 by Yoshiura, Koh-ichiro, Leysens, Nancy J., Reiter, Rebecca S., Murray, Jeffrey C.

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  5. 5
    Cloning, characterization, and mapping of the mouse homeobox gene Hmx1

    Cloning, characterization, and mapping of the mouse homeobox gene Hmx1 by YOSHIURA, K.-I, LEYSENS, N. J, REITER, R. S, MURRAY, J. C

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  6. 6
    Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus

    Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus by SEMINA, E. V, DATSON, N. A, VAN OMMEN, G.-J, MURRAY, J. C, LEYSENS, N. J, ZABEL, B. U, CAREY, J. C, BELL, G. I, BITOUN, P, LINDGREN, C, STEVENSON, T, FRANTS, R. R

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  7. 7
    A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates

    A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates by BUETOW, K. H, SHIANG, R, RITTY, T. M, WISE, M. E, MURRAY, J. C, PING YANG, NAKAMURA, Y, LATHROP, G. M, WHITE, R, WASMUTH, J. J, WOOD, S, BERDAHL, L. D, LEYSENS, N. J

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  8. 8
    Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

    Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes by Yoshiura, Koh-ichiro, Leysens, Nancy J., Chang, Jenny, Ward, Deeann, Murray, Jeffrey C., Muenke, Maximilian

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  9. 9
    Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

    Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes by Yoshiura, Koh-ichiro, Leysens, Nancy J., Chang, Jenny, Ward, Deeann, Murray, Jeffrey C., Muenke, Maximilian

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