Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy von Irvine, Alan D, Corden, Laura D, Swensson, Ole, Swensson, Beate, Moore, Jonathan E, Frazer, David G, Smith, Frances J.D, Knowlton, Robert G, Christophers, Enno, Rochels, Rainer, Uitto, Jouni, McLean, W.H. Irwin

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Genetic Linkage of a Polymorphism in the Type II Procollagen Gene (COL2A1) to Primary Osteoarthritis Associated with Mild Chondrodysplasia von Knowlton, Robert G, Katzenstein, Paul L, Moskowitz, Roland W, Weaver, Eric J, Malemud, Charles J, Pathria, Mini N, Jimenez, Sergio A, Prockop, Darwin J

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Mutations in the Cartilage Oligomeric Matrix Protein (COMP) Gene in Pseudoachondroplasia and Multiple Epiphyseal Dysplasia von Cohn, Daniel H., Briggs, Michael D., King, Lily M., Rimoin, David L., Wilcox, William R., Lachman, Ralph S., Knowlton, Robert G.

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Application of a numerical model for simulating water flow, isotope transport, and heat transfer in the unsaturated zone von Shurbaji, Abdel-Rahman M., Phillips, Fred M., Campbella, Andrew R., Knowlton, Robert G.

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A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 von Knowlton, Robert G, Cohen-Haguenauer, Odile, Van Cong, Nguyen, Frézal, Jean, Brown, Valerie A, Barker, David, Braman, Jeffrey C, Schumm, James W, Tsui, Lap-Chee, Buchwald, Manuel, Donis-Keller, Helen

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Recent Trend for Environmental Compliance Provides New Opportunities for Land and Water Use at Brownfields and Other Contaminated Sites von KNOWLTON, ROBERT G., MINIER, JEFFRIE

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Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum von Briggs, Michael D., Mortier, Geert R., Cole, William G., King, Lily M., Golik, Steven S., Bonaventure, Jacky, Nuytinck, Lieve, De Paepe, Anne, Leroy, Jules G., Biesecker, Leslie, Lipson, Mark, Wilcox, William R., Lachman, Ralph S., Rimoin, David L., Knowlton, Robert G., Cohn, Daniel H.

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Stop Codon in the Procollagen II Gene (COL2A1) in a Family with the Stickler Syndrome (Arthro-Ophthalmopathy) von Ahmad, Nilofer Nina, Ala-Kokko, Leena, Knowlton, Robert G., Jimenez, Sergio A., Weaver, Eric J., Maguire, Joseph I., Tasman, William, Prockop, Darwin J.

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GENETIC-LINKAGE OF RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA TO THE TYPE-VII COLLAGEN GENE von HOVNANIAN, A, DUQUESNOY, P, BLANCHETBARDON, C, KNOWLTON, RG, AMSELEM, S, LATHROP, M, DUBERTRET, L, UITTO, J, GOOSSENS, M

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Human type VII collagen : genetic linkage of the gene (COL7AI) on chromosome 3 to dominant dystrophic epidermolysis bullosa von RYYNÄNEN, M, KNOWLTON, R. G, PARENTE, M. G, CHUNG, L. C, MON-LI CHU, UITTO, J

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GENETIC-LINKAGE OF TYPE-VII COLLAGEN (COL7A1) TO DOMINANT DYSTROPHIC EPIDERMOLYSIS-BULLOSA IN FAMILIES WITH ABNORMAL ANCHORING FIBRILS von RYYNANEN, M, RYYNANEN, J, SOLLBERG, S, IOZZO, RV, KNOWLTON, RG, UITTO, J

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A second mutation in the type II procollagen gene (COL2A1) causing Stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon von AHMAD, N. N, MCDONALD-MCGINN, D. M, ZACKAI, E. H, KNOWLTON, R. G, LAROSSA, D, DIMASCIO, J, PROCKOP, D. J

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Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling von Arbour, Nancy C., Zlotogora, Joel, Knowlton, Robert G., Merin, Saul, Rosenmann, Ada, Kanis, Adam B., Rokhlina, Tatiana, Stone, Edwin M., Sheffield, Val C.

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Mixed Hematopoietic Chimerism Following Bone Marrow Transplantation for Hematologic Malignancies von Petz, Lawrence D., Yam, Priscilla, Wallace, R. Bruce, Stock, A. Dean, Lange, Gerda de, Knowlton, Robert G., Brown, Valerie A., Donis-Keller, Helen, Hill, L. Robert, Forman, Stephen J., Blume, Karl G.

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Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19 von OEHLMANN, R, SUMMERVILLE, G. P, YEH, G, WEAVER, E. J, JIMENEZ, S. A, KNOWLTON, R. G

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Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1) von Williams, C J, Considine, E L, Knowlton, R G, Reginato, A, Neumann, G, Harrison, D, Buxton, P, Jimenez, S, Prockop, D J

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Mapping of epidermolysis bullosa simplex mutation to chromosome 12 von RYYNANEN, M, KNOWLTON, R. G, UITTO, J

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Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia von Loughlin, John, Irven, Catherine, Mustafa, Zehra, Briggs, Michael D., Carr, Andrew, Lynch, Sally-Ann, Knowlton, Robert G., Cohn, Daniel H., Sykes, Bryan

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Localization of the Krabbe disease gene (GALC) on chromosome 14 by multipoint linkage analysis von OEHLMANN, R, ZLOTOGORA, J, WENGER, D. A, KNOWLTON, R. G

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Use of Highly Polymorphic DNA Probes for Genotypic Analysis Following Bone Marrow Transplantation von Knowlton, Robert G., Brown, Valerie A., Braman, Jeffrey C., Barker, David, Schumm, James W., Murray, Christine, Takvorian, Tak, Ritz, Jerome, Donis-Keller, Helen

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