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D F Callen

Showing results (131-140 of 195) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1989
The gene for human carbonic anhydrase VI(CA6) is on the tip of the short arm of chromosome 1G R Sutherland, E Baker, K E Fernandez, et al.
Cancer Genetics and Cytogenetics|January 15, 1998
A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), and enhanced MYC expression in the absence of gene amplificationU R Kees, D Spagnolo, L A Hallam, et al.
Journal of Medical Genetics|October 1, 1993
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotypeD F Callen, H Eyre, S Lane, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisationP A Akkari, H J Eyre, S D Wilton, et al.
Genomics|March 15, 1994
Isolation and characterization of transcribed sequences from a chromosome 16 hn-cDNA library and the physical mapping of genes and transcribed sequences using a high-resolution somatic cell panel of human chromosome 16S A Whitmore, S Apostolou, S Lane, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Human prostate-specific antigen (APS) is a member of the glandular kallikrein gene family at 19q13G R Sutherland, E Baker, V J Hyland, et al.
American Journal of Human Genetics|September 1, 1988
5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemiaG R Sutherland, E Baker, D F Callen, et al.
American Journal of Medical Genetics|November 1, 1993
Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22P Cullen, C S Rodgers, D F Callen, et al.
American Journal of Medical Genetics|June 5, 1995
Phenol sulfotransferases: candidate genes for Batten diseaseT P Dooley, P Probst, R D Obermoeller, et al.
American Journal of Human Genetics|December 1, 1991
Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12D F Callen, E Baker, S Lane, et al.
Pageof 20

Showing results (131-140 of 195) with videos related to

Sort By:
Pageof 20
Cytogenetics and Cell Genetics|January 1, 1989
The gene for human carbonic anhydrase VI(CA6) is on the tip of the short arm of chromosome 1G R Sutherland, E Baker, K E Fernandez, et al.
Cancer Genetics and Cytogenetics|January 15, 1998
A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), and enhanced MYC expression in the absence of gene amplificationU R Kees, D Spagnolo, L A Hallam, et al.
Journal of Medical Genetics|October 1, 1993
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotypeD F Callen, H Eyre, S Lane, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisationP A Akkari, H J Eyre, S D Wilton, et al.
Genomics|March 15, 1994
Isolation and characterization of transcribed sequences from a chromosome 16 hn-cDNA library and the physical mapping of genes and transcribed sequences using a high-resolution somatic cell panel of human chromosome 16S A Whitmore, S Apostolou, S Lane, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Human prostate-specific antigen (APS) is a member of the glandular kallikrein gene family at 19q13G R Sutherland, E Baker, V J Hyland, et al.
American Journal of Human Genetics|September 1, 1988
5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemiaG R Sutherland, E Baker, D F Callen, et al.
American Journal of Medical Genetics|November 1, 1993
Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22P Cullen, C S Rodgers, D F Callen, et al.
American Journal of Medical Genetics|June 5, 1995
Phenol sulfotransferases: candidate genes for Batten diseaseT P Dooley, P Probst, R D Obermoeller, et al.
American Journal of Human Genetics|December 1, 1991
Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12D F Callen, E Baker, S Lane, et al.
Pageof 20