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S W Scherer

Showing results (51-60 of 164) with videos related to

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Human Molecular Genetics|September 25, 1997
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Genome|June 26, 1999
Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymusM Y Hwang, Y J Kang, Y H Kim, et al.
The Journal of Biological Chemistry|August 14, 1999
Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damageA Jilani, D Ramotar, C Slack, et al.
American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.
Genomics|March 1, 1993
Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybridsS W Scherer, E J Neufeld, P M Lievens, et al.
Genomics|January 8, 1999
Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12S Egan, J A Herbrick, L C Tsui, et al.
Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.
Genomics|April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidateC E Tambini, A M George, J M Rommens, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridizationS W Scherer, H H Heng, G W Robinson, et al.
Nature Genetics|November 1, 1996
Mutations in the human Sonic Hedgehog gene cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Pageof 17

Showing results (51-60 of 164) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|September 25, 1997
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Genome|June 26, 1999
Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymusM Y Hwang, Y J Kang, Y H Kim, et al.
The Journal of Biological Chemistry|August 14, 1999
Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damageA Jilani, D Ramotar, C Slack, et al.
American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.
Genomics|March 1, 1993
Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybridsS W Scherer, E J Neufeld, P M Lievens, et al.
Genomics|January 8, 1999
Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12S Egan, J A Herbrick, L C Tsui, et al.
Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.
Genomics|April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidateC E Tambini, A M George, J M Rommens, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridizationS W Scherer, H H Heng, G W Robinson, et al.
Nature Genetics|November 1, 1996
Mutations in the human Sonic Hedgehog gene cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Pageof 17