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M D Briggs

Showing results (1-10 of 23) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|June 7, 2000
Screening for mutations in cartilage ECM genesM D Briggs
Human Molecular Genetics|July 1, 1993
Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) geneM D Briggs, D H Cohn
Journal of Medical Genetics|February 26, 2000
Molecular diagnosis is important to confirm suspected pseudoachondroplasiaB Newman, D Donnah, M D Briggs
European Journal of Human Genetics : EJHG|August 31, 2001
Clinical and radiographic features of multiple epiphyseal dysplasia not linked to the COMP or type IX collagen genesG R Mortier, K Chapman, J L Leroy, et al.
Human Molecular Genetics|January 15, 1999
Trinucleotide expansion mutations in the cartilage oligomeric matrix protein (COMP) geneE Délot, L M King, M D Briggs, et al.
Nature Genetics|August 2, 2001
Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasiaK L Chapman, G R Mortier, K Chapman, et al.
The Journal of Biological Chemistry|November 23, 2000
Cartilage oligomeric matrix protein interacts with type IX collagen, and disruptions to these interactions identify a pathogenetic mechanism in a bone dysplasia familyP Holden, R S Meadows, K L Chapman, 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.
The Journal of Biological Chemistry|January 15, 2000
Identification in vitreous and molecular cloning of opticin, a novel member of the family of leucine-rich repeat proteins of the extracellular matrixA J Reardon, M Le Goff, M D Briggs, 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.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|June 7, 2000
Screening for mutations in cartilage ECM genesM D Briggs
Human Molecular Genetics|July 1, 1993
Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) geneM D Briggs, D H Cohn
Journal of Medical Genetics|February 26, 2000
Molecular diagnosis is important to confirm suspected pseudoachondroplasiaB Newman, D Donnah, M D Briggs
European Journal of Human Genetics : EJHG|August 31, 2001
Clinical and radiographic features of multiple epiphyseal dysplasia not linked to the COMP or type IX collagen genesG R Mortier, K Chapman, J L Leroy, et al.
Human Molecular Genetics|January 15, 1999
Trinucleotide expansion mutations in the cartilage oligomeric matrix protein (COMP) geneE Délot, L M King, M D Briggs, et al.
Nature Genetics|August 2, 2001
Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasiaK L Chapman, G R Mortier, K Chapman, et al.
The Journal of Biological Chemistry|November 23, 2000
Cartilage oligomeric matrix protein interacts with type IX collagen, and disruptions to these interactions identify a pathogenetic mechanism in a bone dysplasia familyP Holden, R S Meadows, K L Chapman, 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.
The Journal of Biological Chemistry|January 15, 2000
Identification in vitreous and molecular cloning of opticin, a novel member of the family of leucine-rich repeat proteins of the extracellular matrixA J Reardon, M Le Goff, M D Briggs, 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.
Pageof 3