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M D Briggs

Showing results (11-20 of 23) with videos related to

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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.
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.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
American Journal of Human Genetics|June 12, 1999
Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasiaP Holden, E G Canty, G R Mortier, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Cell Stress & Chaperones|December 14, 2018
Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasisP A Bell, E P Dennis, C L Hartley, et al.
Pediatric Radiology|February 24, 2001
Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotypeS L Unger, M D Briggs, P Holden, et al.
American Journal of Human Genetics|October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneM D Briggs, H Choi, M L Warman, et al.
Human Genetics|March 1, 1994
A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrixD L Rimoin, I M Rasmussen, M D Briggs, et al.
Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
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.
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.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
American Journal of Human Genetics|June 12, 1999
Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasiaP Holden, E G Canty, G R Mortier, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Cell Stress & Chaperones|December 14, 2018
Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasisP A Bell, E P Dennis, C L Hartley, et al.
Pediatric Radiology|February 24, 2001
Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotypeS L Unger, M D Briggs, P Holden, et al.
American Journal of Human Genetics|October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneM D Briggs, H Choi, M L Warman, et al.
Human Genetics|March 1, 1994
A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrixD L Rimoin, I M Rasmussen, M D Briggs, et al.
Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.
Pageof 3