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C A Francomano

Showing results (31-40 of 101) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2000
A skeletal gene databaseN C Ho, L Jia, C C Driscoll, et al.
Genome Research|May 16, 1998
Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster CountyR Agarwala, L G Biesecker, K A Hopkins, et al.
Neurosurgical Review|January 11, 2019
Cervical medullary syndrome secondary to craniocervical instability and ventral brainstem compression in hereditary hypermobility connective tissue disorders: 5-year follow-up after craniocervical reduction, fusion, and stabilizationFraser C Henderson, C A Francomano, M Koby, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Hypochondroplasia: molecular analysis of the fibroblast growth factor receptor 3 geneG A Bellus, I McIntosh, J Szabo, et al.
Human Molecular Genetics|February 1, 1994
Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locusI McIntosh, M H Abbott, M L Warman, et al.
Human Genetics|November 1, 1996
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the AmishS E Ide, R I Ortiz de Luna, C A Francomano, et al.
Human Genetics|December 1, 1987
Partial structure of the human alpha 2(IV) collagen chain and chromosomal localization of the gene (COL4A2)P D Killen, C A Francomano, Y Yamada, et al.
Human Mutation|January 1, 1992
Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domainsH C Dietz, J M Saraiva, R E Pyeritz, et al.
The Journal of Pediatrics|July 1, 1992
Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infantA Hamosh, J W McDonald, D Valle, et al.
Osteoarthritis and Cartilage|January 18, 2006
Comparison of gene expression profile between human chondrons and chondrocytes: a cDNA microarray studyZ Zhang, J Fan, K G Becker, et al.
Pageof 11

Showing results (31-40 of 101) with videos related to

Sort By:
Pageof 11
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2000
A skeletal gene databaseN C Ho, L Jia, C C Driscoll, et al.
Genome Research|May 16, 1998
Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster CountyR Agarwala, L G Biesecker, K A Hopkins, et al.
Neurosurgical Review|January 11, 2019
Cervical medullary syndrome secondary to craniocervical instability and ventral brainstem compression in hereditary hypermobility connective tissue disorders: 5-year follow-up after craniocervical reduction, fusion, and stabilizationFraser C Henderson, C A Francomano, M Koby, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Hypochondroplasia: molecular analysis of the fibroblast growth factor receptor 3 geneG A Bellus, I McIntosh, J Szabo, et al.
Human Molecular Genetics|February 1, 1994
Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locusI McIntosh, M H Abbott, M L Warman, et al.
Human Genetics|November 1, 1996
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the AmishS E Ide, R I Ortiz de Luna, C A Francomano, et al.
Human Genetics|December 1, 1987
Partial structure of the human alpha 2(IV) collagen chain and chromosomal localization of the gene (COL4A2)P D Killen, C A Francomano, Y Yamada, et al.
Human Mutation|January 1, 1992
Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domainsH C Dietz, J M Saraiva, R E Pyeritz, et al.
The Journal of Pediatrics|July 1, 1992
Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infantA Hamosh, J W McDonald, D Valle, et al.
Osteoarthritis and Cartilage|January 18, 2006
Comparison of gene expression profile between human chondrons and chondrocytes: a cDNA microarray studyZ Zhang, J Fan, K G Becker, et al.
Pageof 11