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Novartis Foundation Symposium
|
March 30, 2001
Defects in extracellular matrix structural proteins in the osteochondrodysplasias
D 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 imperfecta
D H Cohn, P H Byers
Clinics in Perinatology
|
December 1, 1990
Clinical screening for collagen defects in connective tissue diseases
D H Cohn, P H Byers
Gene
|
January 1, 1986
Luciferase genes cloned from the unculturable luminous bacteroid symbiont of the Caribbean flashlight fish, Kryptophanaron alfredi
M 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 imperfecta
D 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 VIIC
A Fujimoto, W R Wilcox, D H Cohn
Science (New York, N.Y.)
|
June 13, 1980
Bacterial origin of luminescence in marine animals
G 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 gene
D 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 I
M C Willing, D H Cohn, P H Byers
Gene
|
December 6, 2001
Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation gene
D Krakow, E Sebald, L M King, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 66) with videos related to
Sort By:
Page
of 7
Novartis Foundation Symposium
|
March 30, 2001
Defects in extracellular matrix structural proteins in the osteochondrodysplasias
D 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 imperfecta
D H Cohn, P H Byers
Clinics in Perinatology
|
December 1, 1990
Clinical screening for collagen defects in connective tissue diseases
D H Cohn, P H Byers
Gene
|
January 1, 1986
Luciferase genes cloned from the unculturable luminous bacteroid symbiont of the Caribbean flashlight fish, Kryptophanaron alfredi
M 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 imperfecta
D 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 VIIC
A Fujimoto, W R Wilcox, D H Cohn
Science (New York, N.Y.)
|
June 13, 1980
Bacterial origin of luminescence in marine animals
G 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 gene
D 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 I
M C Willing, D H Cohn, P H Byers
Gene
|
December 6, 2001
Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation gene
D Krakow, E Sebald, L M King, et al.
Page
of 7