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E Hewitt

Showing results (351-360 of 419) with videos related to

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Human Molecular Genetics|October 1, 1993
Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-regionC Wijmenga, T J Wright, M J Baan, et al.
Ecological Applications : a Publication of the Ecological Society of America|November 29, 2024
Seafloor sediment microtopography as a surrogate for biodiversity and ecosystem functioningStefano Schenone, Judi E Hewitt, Jenny Hillman, et al.
Marine Environmental Research|March 27, 2024
Climatic, oceanic, freshwater, and local environmental drivers of New Zealand estuarine macroinvertebratesOrlando Lam-Gordillo, Judi E Hewitt, Emily J Douglas, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|May 24, 2020
Image-Based Cell Profiling Enables Quantitative Tissue Microscopy in GastroenterologyJohn W Wills, Jack Robertson, Huw D Summers, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Nature Genetics|September 1, 1992
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyC Wijmenga, J E Hewitt, L A Sandkuijl, et al.
Genomics|February 7, 2002
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common originMichel van Geel, Morag C Dickson, Amy F Beck, et al.
Transfusion|February 4, 2016
Virology, serology, and demography of hepatitis E viremic blood donors in South East EnglandRichard S Tedder, Kate I Tettmar, Su R Brailsford, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4qJ Nasir, J L Theilmann, V Chopra, et al.
Human Molecular Genetics|August 1, 1994
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophyJ E Hewitt, R Lyle, L N Clark, et al.
Pageof 42

Showing results (351-360 of 419) with videos related to

Sort By:
Pageof 42
Human Molecular Genetics|October 1, 1993
Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-regionC Wijmenga, T J Wright, M J Baan, et al.
Ecological Applications : a Publication of the Ecological Society of America|November 29, 2024
Seafloor sediment microtopography as a surrogate for biodiversity and ecosystem functioningStefano Schenone, Judi E Hewitt, Jenny Hillman, et al.
Marine Environmental Research|March 27, 2024
Climatic, oceanic, freshwater, and local environmental drivers of New Zealand estuarine macroinvertebratesOrlando Lam-Gordillo, Judi E Hewitt, Emily J Douglas, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|May 24, 2020
Image-Based Cell Profiling Enables Quantitative Tissue Microscopy in GastroenterologyJohn W Wills, Jack Robertson, Huw D Summers, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Nature Genetics|September 1, 1992
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyC Wijmenga, J E Hewitt, L A Sandkuijl, et al.
Genomics|February 7, 2002
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common originMichel van Geel, Morag C Dickson, Amy F Beck, et al.
Transfusion|February 4, 2016
Virology, serology, and demography of hepatitis E viremic blood donors in South East EnglandRichard S Tedder, Kate I Tettmar, Su R Brailsford, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4qJ Nasir, J L Theilmann, V Chopra, et al.
Human Molecular Genetics|August 1, 1994
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophyJ E Hewitt, R Lyle, L N Clark, et al.
Pageof 42