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R G Knowlton

Showing results (61-70 of 88) with videos related to

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Journal of Human Ergology|September 1, 1980
Effects of toeclip use on metabolic and cardiopulmonary responses to bicycle ergometer exerciseS W Wilde, R G Knowlton, D S Miles, et al.
American Journal of Human Genetics|January 1, 1994
Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19R Oehlmann, G P Summerville, G Yeh, et al.
American Journal of Human Genetics|October 1, 1991
Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosaM Ryynänen, R G Knowlton, M G Parente, et al.
International Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Influence of age on caloric expenditure during exerciseS M Somani, P Buckenmeyer, S N Dube, et al.
American Journal of Medical Genetics|February 11, 1997
Multiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African familyR Ballo, M D Briggs, D H Cohn, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Highly polymorphic RFLP probes as diagnostic toolsH Donis-Keller, D F Barker, R G Knowlton, et al.
Genomics|December 1, 1991
Bullous pemphigoid antigens (BPAGs): identification of RFLPs in human BPAG1 and BPAG2, and exclusion as candidate genes in a large kindred with dominant epidermolysis bullosa simplexM Ryynänen, R G Knowlton, M Kero, et al.
American Journal of Human Genetics|January 1, 1993
A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codonN N Ahmad, D M McDonald-McGinn, E H Zackai, et al.
The Journal of Clinical Investigation|September 1, 1992
Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen geneA Hovnanian, P Duquesnoy, C Blanchet-Bardon, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Mutations in the cartilage oligomeric matrix protein (COMP) gene in pseudoachondroplasia and multiple epiphyseal dysplasiaD H Cohn, M D Briggs, L M King, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Journal of Human Ergology|September 1, 1980
Effects of toeclip use on metabolic and cardiopulmonary responses to bicycle ergometer exerciseS W Wilde, R G Knowlton, D S Miles, et al.
American Journal of Human Genetics|January 1, 1994
Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19R Oehlmann, G P Summerville, G Yeh, et al.
American Journal of Human Genetics|October 1, 1991
Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosaM Ryynänen, R G Knowlton, M G Parente, et al.
International Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Influence of age on caloric expenditure during exerciseS M Somani, P Buckenmeyer, S N Dube, et al.
American Journal of Medical Genetics|February 11, 1997
Multiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African familyR Ballo, M D Briggs, D H Cohn, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Highly polymorphic RFLP probes as diagnostic toolsH Donis-Keller, D F Barker, R G Knowlton, et al.
Genomics|December 1, 1991
Bullous pemphigoid antigens (BPAGs): identification of RFLPs in human BPAG1 and BPAG2, and exclusion as candidate genes in a large kindred with dominant epidermolysis bullosa simplexM Ryynänen, R G Knowlton, M Kero, et al.
American Journal of Human Genetics|January 1, 1993
A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codonN N Ahmad, D M McDonald-McGinn, E H Zackai, et al.
The Journal of Clinical Investigation|September 1, 1992
Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen geneA Hovnanian, P Duquesnoy, C Blanchet-Bardon, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Mutations in the cartilage oligomeric matrix protein (COMP) gene in pseudoachondroplasia and multiple epiphyseal dysplasiaD H Cohn, M D Briggs, L M King, et al.
Pageof 9