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W J Craigen

Showing results (31-40 of 53) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 1999
Revised fine mapping of the human voltage-dependent anion channel loci by radiation hybrid analysisW K Decker, K R Bowles, E C Schatte, et al.
Human Genetics|September 12, 2000
Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VIIM L Raff, W J Craigen, L T Smith, et al.
Journal of Bacteriology|October 1, 1988
Rapid and precise mapping of the Escherichia coli release factor genes by two physical approachesC C Lee, Y Kohara, K Akiyama, et al.
The Journal of Biological Chemistry|August 25, 1990
Ectopic correction of ornithine transcarbamylase deficiency in sparse fur miceS N Jones, M Grompe, M I Munir, et al.
Journal of Medical Genetics|September 9, 2000
Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assayK Kosaki, R Kosaki, W P Robinson, et al.
American Journal of Human Genetics|June 19, 1998
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile ciliaY Pan, C D McCaskill, K H Thompson, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
American Journal of Medical Genetics|August 1, 1994
De novo proximal interstitial deletions of 14q: cytogenetic and molecular investigationsS K Shapira, K L Anderson, A Orr-Urtregar, et al.
Clinical Genetics|July 16, 2004
Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndromeS A Yatsenko, A N Yatsenko, K Szigeti, et al.
The Journal of Biological Chemistry|August 17, 2001
Immotile sperm and infertility in mice lacking mitochondrial voltage-dependent anion channel type 3M J Sampson, W K Decker, A L Beaudet, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 1999
Revised fine mapping of the human voltage-dependent anion channel loci by radiation hybrid analysisW K Decker, K R Bowles, E C Schatte, et al.
Human Genetics|September 12, 2000
Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VIIM L Raff, W J Craigen, L T Smith, et al.
Journal of Bacteriology|October 1, 1988
Rapid and precise mapping of the Escherichia coli release factor genes by two physical approachesC C Lee, Y Kohara, K Akiyama, et al.
The Journal of Biological Chemistry|August 25, 1990
Ectopic correction of ornithine transcarbamylase deficiency in sparse fur miceS N Jones, M Grompe, M I Munir, et al.
Journal of Medical Genetics|September 9, 2000
Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assayK Kosaki, R Kosaki, W P Robinson, et al.
American Journal of Human Genetics|June 19, 1998
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile ciliaY Pan, C D McCaskill, K H Thompson, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
American Journal of Medical Genetics|August 1, 1994
De novo proximal interstitial deletions of 14q: cytogenetic and molecular investigationsS K Shapira, K L Anderson, A Orr-Urtregar, et al.
Clinical Genetics|July 16, 2004
Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndromeS A Yatsenko, A N Yatsenko, K Szigeti, et al.
The Journal of Biological Chemistry|August 17, 2001
Immotile sperm and infertility in mice lacking mitochondrial voltage-dependent anion channel type 3M J Sampson, W K Decker, A L Beaudet, et al.
Pageof 6