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R G Knowlton

Showing results (71-80 of 88) with videos related to

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American Journal of Medical Genetics|February 1, 1993
Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasiaE J Weaver, G P Summerville, G Yeh, et al.
Genomics|August 10, 1995
High-resolution genetic and physical mapping of multiple epiphyseal dysplasia and pseudoachondroplasia mutations at chromosome 19p13.1-p12R G Knowlton, J A Cekleniak, D H Cohn, et al.
Human Mutation|February 6, 1998
Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasiaJ Loughlin, C Irven, Z Mustafa, et al.
Human Genetics|November 1, 1993
Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1)C J Williams, E L Considine, R G Knowlton, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)N N Ahmad, L Ala-Kokko, R G Knowlton, et al.
Blood|August 1, 1986
Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplantationR G Knowlton, V A Brown, J C Braman, et al.
Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.
The New England Journal of Medicine|February 22, 1990
Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasiaR G Knowlton, P L Katzenstein, R W Moskowitz, et al.
American Journal of Human Genetics|January 1, 1988
Identification of more than 500 RFLPs by screening random genomic clonesJ W Schumm, R G Knowlton, J C Braman, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Chromosomal assignment of 14 genomic probes for highly polymorphic lociO Cohen-Haguenauer, Nguyen Van Cong, R G Knowlton, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|February 1, 1993
Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasiaE J Weaver, G P Summerville, G Yeh, et al.
Genomics|August 10, 1995
High-resolution genetic and physical mapping of multiple epiphyseal dysplasia and pseudoachondroplasia mutations at chromosome 19p13.1-p12R G Knowlton, J A Cekleniak, D H Cohn, et al.
Human Mutation|February 6, 1998
Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasiaJ Loughlin, C Irven, Z Mustafa, et al.
Human Genetics|November 1, 1993
Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1)C J Williams, E L Considine, R G Knowlton, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)N N Ahmad, L Ala-Kokko, R G Knowlton, et al.
Blood|August 1, 1986
Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplantationR G Knowlton, V A Brown, J C Braman, et al.
Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.
The New England Journal of Medicine|February 22, 1990
Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasiaR G Knowlton, P L Katzenstein, R W Moskowitz, et al.
American Journal of Human Genetics|January 1, 1988
Identification of more than 500 RFLPs by screening random genomic clonesJ W Schumm, R G Knowlton, J C Braman, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Chromosomal assignment of 14 genomic probes for highly polymorphic lociO Cohen-Haguenauer, Nguyen Van Cong, R G Knowlton, et al.
Pageof 9