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C M Eng

Showing results (1-10 of 35) with videos related to

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Prenatal Diagnosis|March 12, 1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosisF H Fodor, C M Eng
Human Mutation|January 1, 1994
Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A geneC M Eng, R J Desnick
Advances in Genetics|October 13, 2001
Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseasesC M Eng, R J Desnick
Genomics|April 1, 1992
Invariant exon skipping in the human alpha-galactosidase A pre-mRNA: Ag+1 to t substitution in a 5'-splice site causing Fabry diseaseH Sakuraba, C M Eng, R J Desnick, et al.
American Journal of Medical Genetics|August 22, 1997
Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1M Caggana, G A Ashley, R J Desnick, et al.
Prenatal Diagnosis|April 1, 1996
Molecular prenatal diagnosis of glycogen storage disease type IaY Qu, J E Abdenur, C M Eng, et al.
Genomics|November 1, 1992
Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellumC M Eng, B A Durtschi, H Y Zoghbi, et al.
The Journal of Experimental Biology|December 1, 2009
The morphology of the masticatory apparatus facilitates muscle force production at wide jaw gapes in tree-gouging common marmosets (Callithrix jacchus)C M Eng, S R Ward, C J Vinyard, et al.
Genomics|February 1, 1991
Mapping of multiple subunits of the neuronal nicotinic acetylcholine receptor to chromosome 15 in man and chromosome 9 in mouseC M Eng, C A Kozak, A L Beaudet, et al.
Molecular Genetics and Metabolism|June 2, 2001
Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi JewsJ Dong, D R Katz, C M Eng, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|March 12, 1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosisF H Fodor, C M Eng
Human Mutation|January 1, 1994
Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A geneC M Eng, R J Desnick
Advances in Genetics|October 13, 2001
Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseasesC M Eng, R J Desnick
Genomics|April 1, 1992
Invariant exon skipping in the human alpha-galactosidase A pre-mRNA: Ag+1 to t substitution in a 5'-splice site causing Fabry diseaseH Sakuraba, C M Eng, R J Desnick, et al.
American Journal of Medical Genetics|August 22, 1997
Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1M Caggana, G A Ashley, R J Desnick, et al.
Prenatal Diagnosis|April 1, 1996
Molecular prenatal diagnosis of glycogen storage disease type IaY Qu, J E Abdenur, C M Eng, et al.
Genomics|November 1, 1992
Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellumC M Eng, B A Durtschi, H Y Zoghbi, et al.
The Journal of Experimental Biology|December 1, 2009
The morphology of the masticatory apparatus facilitates muscle force production at wide jaw gapes in tree-gouging common marmosets (Callithrix jacchus)C M Eng, S R Ward, C J Vinyard, et al.
Genomics|February 1, 1991
Mapping of multiple subunits of the neuronal nicotinic acetylcholine receptor to chromosome 15 in man and chromosome 9 in mouseC M Eng, C A Kozak, A L Beaudet, et al.
Molecular Genetics and Metabolism|June 2, 2001
Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi JewsJ Dong, D R Katz, C M Eng, et al.
Pageof 4