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C A Stolle

Showing results (1-10 of 30) with videos related to

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Gene|January 1, 1988
Cellular factor affecting the stability of beta-globin mRNAC A Stolle, E J Benz
American Journal of Human Genetics|October 30, 1998
A new twist: some patients with Saethre-Chotzen syndrome have a microdeletion syndromeE H Zackai, C A Stolle
Blood|July 1, 1987
Equal stabilities of normal beta globin and nontranslatable beta0 -39 thalassemic transcripts in cell-free extractsC A Stolle, M S Payne, E J Benz
Human Mutation|January 1, 1997
Recurrent COL3A1 mutation results in EDS IV or familial aneurysmsD W Anderson, S Thakker-Varia, C A Stolle
Annals of the New York Academy of Sciences|November 18, 1996
Phenotypic overlap between familial aneurysms and Ehlers-Danlos syndrome type IV resulting from a type III procollagen gene mutationD W Anderson, S Thakker-Varia, C A Stolle
American Journal of Medical Genetics|May 8, 2000
Craniosynostosis: molecular testing-a necessity for counselingE H Zackai, K W Gripp, C A Stolle
Human Mutation|January 29, 2000
Mutations in the human TWIST geneK W Gripp, E H Zackai, C A Stolle
Gene|February 28, 1997
Characterization of the rat carbonic anhydrase II gene structure: sequence analysis of the 5' flanking region and 3' UTRM H McGowan, J A Neubauer, C A Stolle
Methods in Molecular Medicine|February 15, 2011
Molecular analysis of the von hippel-lindau disease geneA Chernoff, V Kasparcova, W M Linehan, et al.
The Journal of Biological Chemistry|May 10, 1985
Partial covalent structure of the human alpha 2 type V collagen chainJ C Myers, H R Loidl, C A Stolle, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Gene|January 1, 1988
Cellular factor affecting the stability of beta-globin mRNAC A Stolle, E J Benz
American Journal of Human Genetics|October 30, 1998
A new twist: some patients with Saethre-Chotzen syndrome have a microdeletion syndromeE H Zackai, C A Stolle
Blood|July 1, 1987
Equal stabilities of normal beta globin and nontranslatable beta0 -39 thalassemic transcripts in cell-free extractsC A Stolle, M S Payne, E J Benz
Human Mutation|January 1, 1997
Recurrent COL3A1 mutation results in EDS IV or familial aneurysmsD W Anderson, S Thakker-Varia, C A Stolle
Annals of the New York Academy of Sciences|November 18, 1996
Phenotypic overlap between familial aneurysms and Ehlers-Danlos syndrome type IV resulting from a type III procollagen gene mutationD W Anderson, S Thakker-Varia, C A Stolle
American Journal of Medical Genetics|May 8, 2000
Craniosynostosis: molecular testing-a necessity for counselingE H Zackai, K W Gripp, C A Stolle
Human Mutation|January 29, 2000
Mutations in the human TWIST geneK W Gripp, E H Zackai, C A Stolle
Gene|February 28, 1997
Characterization of the rat carbonic anhydrase II gene structure: sequence analysis of the 5' flanking region and 3' UTRM H McGowan, J A Neubauer, C A Stolle
Methods in Molecular Medicine|February 15, 2011
Molecular analysis of the von hippel-lindau disease geneA Chernoff, V Kasparcova, W M Linehan, et al.
The Journal of Biological Chemistry|May 10, 1985
Partial covalent structure of the human alpha 2 type V collagen chainJ C Myers, H R Loidl, C A Stolle, et al.
Pageof 3