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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Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene von Briggs, M.D, Hoffman, S.M.G, King, L.M, Olsen, A.S, Mohrenweiser, H, Leroy, J.G, Mortier, G.R, Rimoin, D.L, Lachman, R.S, Gaines, E.S, Cekleniak, J.A, Knowlton, R.G, Cohn, D.H

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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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Effects of dehydration on isometric muscular strength and endurance von GREIWE, J. S, STAFFEY, K. S, MELROSE, D. R, NARVE, M. D, KNOWLTON, R. G

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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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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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ACCURACY OF RPE FROM GRADED-EXERCISE TO ESTABLISH EXERCISE TRAINING INTENSITY von GLASS, SC, KNOWLTON, RG, BECQUE, MD

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

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Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene von KNOWLTON, R. G, WEAVER, E. J, STRUYK, A. F, KNOBLOCH, W. H, KING, R. A, NORRIS, K, SHAMBAN, A, UITTO, J, JIMENEZ, S. A, PROCKOP, D. J

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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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Identification of more than 500 RFLPs by screening random genomic clones von SCHUMM, J. W, KNOWLTON, R. G, REDIKER, K, THURSTON, J. G, DONIS-KELLER, H, BRAMAN, J. C, BARKER, D. F, BOTSTEIN, D, AKOTS, G, BROWN, V. A, GRAVIUS, T. C, HELMS, C, HSIAO, K

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An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome von KNOWLTON, R. G, NELSON, C. A, BROWN, V. A, PAGE, D. C, DONIS-KELLER, H

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Prenatal exclusion of stickler syndrome von Zlotogora, Joel, Granat, Menachem, Knowlton, Robert G.

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Perception of effort during high-intensity exercise at low, moderate and high wet bulb globe temperatures von GLASS, S. C, KNOWLTON, R. G, BECQUE, M. D

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Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster von Pulkkinen, L, Christiano, A M, Knowlton, R G, Uitto, J

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