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D H Cohn

Showing results (1-10 of 66) with videos related to

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Novartis Foundation Symposium|March 30, 2001
Defects in extracellular matrix structural proteins in the osteochondrodysplasiasD H Cohn
Human Genetics|June 1, 1991
Cysteine in the triple helical domain of the pro alpha 2(I) chain of type-I collagen in nonlethal forms of osteogenesis imperfectaD H Cohn, P H Byers
Clinics in Perinatology|December 1, 1990
Clinical screening for collagen defects in connective tissue diseasesD H Cohn, P H Byers
Gene|January 1, 1986
Luciferase genes cloned from the unculturable luminous bacteroid symbiont of the Caribbean flashlight fish, Kryptophanaron alfrediM G Haygood, D H Cohn
Human Mutation|January 1, 1993
Homology-mediated recombination between type I collagen gene exons results in an internal tandem duplication and lethal osteogenesis imperfectaD H Cohn, X Zhang, P H Byers
American Journal of Medical Genetics|January 10, 1997
Clinical, morphological, and biochemical phenotype of a new case of Ehlers-Danlos syndrome type VIICA Fujimoto, W R Wilcox, D H Cohn
Science (New York, N.Y.)|June 13, 1980
Bacterial origin of luminescence in marine animalsG Leisman, D H Cohn, K H Nealson
Genomics|February 1, 1993
Heteroduplex analysis can increase the informativeness of PCR-amplified VNTR markers: application using a marker tightly linked to the COL2A1 geneD J Wilkin, K E Koprivnikar, D H Cohn
The Journal of Clinical Investigation|January 1, 1990
Frameshift mutation near the 3' end of the COL1A1 gene of type I collagen predicts an elongated Pro alpha 1(I) chain and results in osteogenesis imperfecta type IM C Willing, D H Cohn, P H Byers
Gene|December 6, 2001
Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation geneD Krakow, E Sebald, L M King, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Novartis Foundation Symposium|March 30, 2001
Defects in extracellular matrix structural proteins in the osteochondrodysplasiasD H Cohn
Human Genetics|June 1, 1991
Cysteine in the triple helical domain of the pro alpha 2(I) chain of type-I collagen in nonlethal forms of osteogenesis imperfectaD H Cohn, P H Byers
Clinics in Perinatology|December 1, 1990
Clinical screening for collagen defects in connective tissue diseasesD H Cohn, P H Byers
Gene|January 1, 1986
Luciferase genes cloned from the unculturable luminous bacteroid symbiont of the Caribbean flashlight fish, Kryptophanaron alfrediM G Haygood, D H Cohn
Human Mutation|January 1, 1993
Homology-mediated recombination between type I collagen gene exons results in an internal tandem duplication and lethal osteogenesis imperfectaD H Cohn, X Zhang, P H Byers
American Journal of Medical Genetics|January 10, 1997
Clinical, morphological, and biochemical phenotype of a new case of Ehlers-Danlos syndrome type VIICA Fujimoto, W R Wilcox, D H Cohn
Science (New York, N.Y.)|June 13, 1980
Bacterial origin of luminescence in marine animalsG Leisman, D H Cohn, K H Nealson
Genomics|February 1, 1993
Heteroduplex analysis can increase the informativeness of PCR-amplified VNTR markers: application using a marker tightly linked to the COL2A1 geneD J Wilkin, K E Koprivnikar, D H Cohn
The Journal of Clinical Investigation|January 1, 1990
Frameshift mutation near the 3' end of the COL1A1 gene of type I collagen predicts an elongated Pro alpha 1(I) chain and results in osteogenesis imperfecta type IM C Willing, D H Cohn, P H Byers
Gene|December 6, 2001
Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation geneD Krakow, E Sebald, L M King, et al.
Pageof 7