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D H Cohn

Showing results (61-70 of 66) with videos related to

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Nature Genetics|October 15, 1998
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouseM Faiyaz ul Haque, L M King, D Krakow, et al.
American Journal of Human Genetics|July 27, 1999
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.
Journal of Medical Genetics|April 3, 2004
A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14C Steiner, N Ehtesham, K D Taylor, et al.
Nature Genetics|March 18, 1999
Heterozygous mutations in the gene encoding noggin affect human joint morphogenesisY Gong, D Krakow, J Marcelino, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 28, 2013
Next-generation sequencing for disorders of low and high bone mineral densityG Sule, P M Campeau, V W Zhang, et al.
American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Nature Genetics|October 15, 1998
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouseM Faiyaz ul Haque, L M King, D Krakow, et al.
American Journal of Human Genetics|July 27, 1999
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.
Journal of Medical Genetics|April 3, 2004
A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14C Steiner, N Ehtesham, K D Taylor, et al.
Nature Genetics|March 18, 1999
Heterozygous mutations in the gene encoding noggin affect human joint morphogenesisY Gong, D Krakow, J Marcelino, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 28, 2013
Next-generation sequencing for disorders of low and high bone mineral densityG Sule, P M Campeau, V W Zhang, et al.
American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.
Pageof 7