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E Roessler

Showing results (61-70 of 76) with videos related to

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Diabetes|December 1, 1990
Mild hypoglycemia and impairment of brain stem and cortical evoked potentials in healthy subjectsT W Jones, G McCarthy, W V Tamborlane, et al.
Beilstein Journal of Organic Chemistry|December 15, 2015
Hexacoordinate Ru-based olefin metathesis catalysts with pH-responsive N-heterocyclic carbene (NHC) and N-donor ligands for ROMP reactions in non-aqueous, aqueous and emulsion conditionsShawna L Balof, K Owen Nix, Matthew S Olliff, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
Nature Genetics|June 3, 2000
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determinationK W Gripp, D Wotton, M C Edwards, et al.
Molecular Syndromology|May 9, 2013
Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL AssociationB D Solomon, D E Pineda-Alvarez, D W Hadley, et al.
American Journal of Human Genetics|October 10, 2007
Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humansJ D Karkera, J S Lee, E Roessler, et al.
Nature Genetics|November 4, 2000
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsR N Bamford, E Roessler, R D Burdine, et al.
Nature Genetics|November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephalyE Belloni, M Muenke, E Roessler, et al.
Human Molecular Genetics|November 11, 1999
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephalyL Nanni, J E Ming, M Bocian, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Diabetes|December 1, 1990
Mild hypoglycemia and impairment of brain stem and cortical evoked potentials in healthy subjectsT W Jones, G McCarthy, W V Tamborlane, et al.
Beilstein Journal of Organic Chemistry|December 15, 2015
Hexacoordinate Ru-based olefin metathesis catalysts with pH-responsive N-heterocyclic carbene (NHC) and N-donor ligands for ROMP reactions in non-aqueous, aqueous and emulsion conditionsShawna L Balof, K Owen Nix, Matthew S Olliff, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
Nature Genetics|June 3, 2000
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determinationK W Gripp, D Wotton, M C Edwards, et al.
Molecular Syndromology|May 9, 2013
Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL AssociationB D Solomon, D E Pineda-Alvarez, D W Hadley, et al.
American Journal of Human Genetics|October 10, 2007
Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humansJ D Karkera, J S Lee, E Roessler, et al.
Nature Genetics|November 4, 2000
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsR N Bamford, E Roessler, R D Burdine, et al.
Nature Genetics|November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephalyE Belloni, M Muenke, E Roessler, et al.
Human Molecular Genetics|November 11, 1999
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephalyL Nanni, J E Ming, M Bocian, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Pageof 8