Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene von KASTURY, K, TAYLOR, W. E, SHEN, R, ARVER, S, GUTIERREZ, M, FISHER, C. E, COUCKE, P. J, VAN HAUWE, P, VAN CAMP, G, BHASIN, S

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The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q von Coucke, Paul, Van Camp, Guy, Demirhan, Osman, Kabakkaya, Yilmaz, Balemans, Wendy, Van Hauwe, Peter, Van Agtmael, Tom, Smith, Richard J.H., Parving, Agnete, Bolder, Cuny H.H.M., Cremers, Cor W.R.J., Willems, Patrick J.

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Chromosomal Mapping of Two Members of the Human Dynein Gene Family to Chromosome Regions 7p15 and 11q13 near the Deafness Loci DFNA 5 and DFNA 11 von Kastury, Kumar, Taylor, Wayne E., Gutierrez, Matthew, Ramirez, Luz, Coucke, Paul J., Van Hauwe, Peter, Van Camp, Guy, Bhasin, Shalender

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Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene von Kastury, K, Taylor, WE, Shen, RQ, Arver, S, Gutierrez, M, Fisher, CE, Coucke, PJ, VanHauwe, P, VanCamp, G, Bhasin, S

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RP4::Mu3A-mediated in vivo cloning and transfer of a chlorobiphenyl catabolic pathway von Springael, Dirk, van Thor, Jasper, Goorissen, Heleen, Ryngaert, Annemie, De Baere, Raymond, Van Hauwe, Peter, Commandeur, Laetitia C. M, Parsons, John R, De Wachter, Rupert, Mergeay, Max

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New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p von Chen, Achih, Wayne, Sigrid, Bell, Adam, Ramesh, Arabandi, Srisailapathy, C.R. Srikumari, Scott, Daryl A., Sheffield, Val C., Hauwe, Peter Van, Zbar, Ross I. S., Ashley, Jennifer, Lovett, Michael, Camp, Guy Van, Smith, Richard J. H.

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