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G B Collin

Showing results (1-10 of 12) with videos related to

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APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 3, 1998
Testicular teratocarcinogenesis in mice--a reviewA Matin, G B Collin, D S Varnum, et al.
Nature Genetics|October 3, 1999
Susceptibility to testicular germ-cell tumours in a 129.MOLF-Chr 19 chromosome substitution strainA Matin, G B Collin, Y Asada, et al.
Genomics|November 4, 1998
Human DCTN1: genomic structure and evaluation as a candidate for Alström syndromeG B Collin, P M Nishina, J D Marshall, et al.
Human Molecular Genetics|February 1, 1997
Homozygosity mapping at Alström syndrome to chromosome 2pG B Collin, J D Marshall, L R Cardon, et al.
Genomics|October 1, 1996
Physical and genetic mapping of novel microsatellite polymorphisms on human chromosome 19G B Collin, A Münch, J L Mu, et al.
Scientific Reports|March 30, 2020
Disruption in murine Eml1 perturbs retinal lamination during early developmentG B Collin, J Won, M P Krebs, et al.
Genomics|June 2, 2001
Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndromeF Chen, G B Collin, K C Liu, et al.
Clinical Genetics|September 14, 2007
Molecular analysis and long-term clinical evaluation of three siblings with Alström syndromeR K Ozgül, I Satman, G B Collin, et al.
Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.
Journal of Lipid Research|July 7, 1999
Quantitative trait loci analysis for the differences in susceptibility to atherosclerosis and diabetes between inbred mouse strains C57BL/6J and C57BLKS/JJ L Mu, J K Naggert, K L Svenson, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|April 3, 1998
Testicular teratocarcinogenesis in mice--a reviewA Matin, G B Collin, D S Varnum, et al.
Nature Genetics|October 3, 1999
Susceptibility to testicular germ-cell tumours in a 129.MOLF-Chr 19 chromosome substitution strainA Matin, G B Collin, Y Asada, et al.
Genomics|November 4, 1998
Human DCTN1: genomic structure and evaluation as a candidate for Alström syndromeG B Collin, P M Nishina, J D Marshall, et al.
Human Molecular Genetics|February 1, 1997
Homozygosity mapping at Alström syndrome to chromosome 2pG B Collin, J D Marshall, L R Cardon, et al.
Genomics|October 1, 1996
Physical and genetic mapping of novel microsatellite polymorphisms on human chromosome 19G B Collin, A Münch, J L Mu, et al.
Scientific Reports|March 30, 2020
Disruption in murine Eml1 perturbs retinal lamination during early developmentG B Collin, J Won, M P Krebs, et al.
Genomics|June 2, 2001
Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndromeF Chen, G B Collin, K C Liu, et al.
Clinical Genetics|September 14, 2007
Molecular analysis and long-term clinical evaluation of three siblings with Alström syndromeR K Ozgül, I Satman, G B Collin, et al.
Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.
Journal of Lipid Research|July 7, 1999
Quantitative trait loci analysis for the differences in susceptibility to atherosclerosis and diabetes between inbred mouse strains C57BL/6J and C57BLKS/JJ L Mu, J K Naggert, K L Svenson, et al.
Pageof 2