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D F Callen

Showing results (121-130 of 195) with videos related to

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Genomics|October 1, 1993
Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16Z Deng, P Liu, P Marlton, et al.
American Journal of Human Genetics|May 1, 1993
Incidence and origin of "null" alleles in the (AC)n microsatellite markersD F Callen, A D Thompson, Y Shen, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridizationS D Wilton, L Lim, S D Dorosz, et al.
Human Genetics|September 10, 1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7C Settasatian, S A Whitmore, J Crawford, et al.
Genomics|November 1, 1991
Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1H M Kozman, A K Gedeon, S Whitmore, et al.
Journal of Medical Genetics|February 1, 1995
Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivationD F Callen, H J Eyre, G Dolman, et al.
Leukemia|October 1, 1993
Identification of an inversion 16 coexisting with an isochromosome 22q by in situ hybridization in a case of childhood AML M4eS G Gad, D F Callen, B Kuss, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Chromosomal location of the human transketolase geneN M Lapsys, R Layfield, E Baker, et al.
Journal of Medical Genetics|November 2, 1999
Origins of accessory small ring marker chromosomes derived from chromosome 1D F Callen, H Eyre, Y Y Fang, et al.
American Journal of Medical Genetics|February 1, 1991
Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28B A Oostra, D F Majoor-Krakauer, J O van Hemel, et al.
Pageof 20

Showing results (121-130 of 195) with videos related to

Sort By:
Pageof 20
Genomics|October 1, 1993
Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16Z Deng, P Liu, P Marlton, et al.
American Journal of Human Genetics|May 1, 1993
Incidence and origin of "null" alleles in the (AC)n microsatellite markersD F Callen, A D Thompson, Y Shen, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridizationS D Wilton, L Lim, S D Dorosz, et al.
Human Genetics|September 10, 1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7C Settasatian, S A Whitmore, J Crawford, et al.
Genomics|November 1, 1991
Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1H M Kozman, A K Gedeon, S Whitmore, et al.
Journal of Medical Genetics|February 1, 1995
Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivationD F Callen, H J Eyre, G Dolman, et al.
Leukemia|October 1, 1993
Identification of an inversion 16 coexisting with an isochromosome 22q by in situ hybridization in a case of childhood AML M4eS G Gad, D F Callen, B Kuss, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Chromosomal location of the human transketolase geneN M Lapsys, R Layfield, E Baker, et al.
Journal of Medical Genetics|November 2, 1999
Origins of accessory small ring marker chromosomes derived from chromosome 1D F Callen, H Eyre, Y Y Fang, et al.
American Journal of Medical Genetics|February 1, 1991
Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28B A Oostra, D F Majoor-Krakauer, J O van Hemel, et al.
Pageof 20