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H M Dahl

Showing results (1-10 of 7) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1995
[Ascent of the testis]H M Dahl, T K Nerhus, O S Haga, et al.
Biochimica Et Biophysica Acta|April 13, 2000
Cloning, mapping and expression analysis of the sheep Wilson disease gene homologueP J Lockhart, S A Wilcox, H M Dahl, et al.
Nucleic Acids Research|June 11, 1981
The structure of a thirty-six kilobase region of the human chromosome including the fibroblast interferon gene IFN-betaG Gross, U Mayr, W Bruns, et al.
Pediatric Dentistry|October 6, 1999
Tooth root resorption associated with a familial bone dysplasia affecting mother and daughterC B Olsen, K Tangchaitrong, I Chippendale, et al.
Prenatal Diagnosis|December 11, 1999
Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNAS L White, S Shanske, I Biros, et al.
Trends in Genetics : TIG|November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?P F Chinnery, D R Thorburn, D C Samuels, et al.
Journal of Medical Genetics|July 15, 2006
The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school childrenH-H M Dahl, S E Tobin, Z Poulakis, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1995
[Ascent of the testis]H M Dahl, T K Nerhus, O S Haga, et al.
Biochimica Et Biophysica Acta|April 13, 2000
Cloning, mapping and expression analysis of the sheep Wilson disease gene homologueP J Lockhart, S A Wilcox, H M Dahl, et al.
Nucleic Acids Research|June 11, 1981
The structure of a thirty-six kilobase region of the human chromosome including the fibroblast interferon gene IFN-betaG Gross, U Mayr, W Bruns, et al.
Pediatric Dentistry|October 6, 1999
Tooth root resorption associated with a familial bone dysplasia affecting mother and daughterC B Olsen, K Tangchaitrong, I Chippendale, et al.
Prenatal Diagnosis|December 11, 1999
Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNAS L White, S Shanske, I Biros, et al.
Trends in Genetics : TIG|November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?P F Chinnery, D R Thorburn, D C Samuels, et al.
Journal of Medical Genetics|July 15, 2006
The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school childrenH-H M Dahl, S E Tobin, Z Poulakis, et al.
Pageof 1