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D F Callen

Showing results (111-120 of 195) with videos related to

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American Journal of Human Genetics|September 1, 1990
The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridizationD F Callen, C J Freemantle, M L Ringenbergs, et al.
Oncogene|October 12, 2011
Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11J E Noll, J Jeffery, F Al-Ejeh, et al.
Biochemical and Biophysical Research Communications|March 15, 1994
Chromosomal assignment of the human SA gene to 16p13.11 and demonstration of its expression in the kidneyN J Samani, S A Whitmore, M A Kaiser, et al.
Human Genetics|August 1, 1989
Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and XV J Hyland, K E Fernandez, D F Callen, et al.
American Journal of Human Genetics|November 1, 1995
Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4Y Y Fang, H J Eyre, S K Bohlander, et al.
Nucleic Acids Research|October 25, 1991
An STS at the D16S290 locusL Z Chen, Y Shen, K Holman, et al.
American Journal of Human Genetics|January 1, 1993
The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3E Baker, X H Guo, A M Orsborn, et al.
Cytogenetics and Cell Genetics|January 1, 1986
A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) lociA Fratini, R N Simmers, D F Callen, et al.
Genomics|December 1, 1993
Identification and regional localization of a human IMP dehydrogenase-like locus (IMPDHL1) at 16p13.13N A Doggett, D F Callen, Z L Chen, et al.
Genomics|February 1, 1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16D F Callen, V J Hyland, E G Baker, et al.
Pageof 20

Showing results (111-120 of 195) with videos related to

Sort By:
Pageof 20
American Journal of Human Genetics|September 1, 1990
The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridizationD F Callen, C J Freemantle, M L Ringenbergs, et al.
Oncogene|October 12, 2011
Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11J E Noll, J Jeffery, F Al-Ejeh, et al.
Biochemical and Biophysical Research Communications|March 15, 1994
Chromosomal assignment of the human SA gene to 16p13.11 and demonstration of its expression in the kidneyN J Samani, S A Whitmore, M A Kaiser, et al.
Human Genetics|August 1, 1989
Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and XV J Hyland, K E Fernandez, D F Callen, et al.
American Journal of Human Genetics|November 1, 1995
Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4Y Y Fang, H J Eyre, S K Bohlander, et al.
Nucleic Acids Research|October 25, 1991
An STS at the D16S290 locusL Z Chen, Y Shen, K Holman, et al.
American Journal of Human Genetics|January 1, 1993
The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3E Baker, X H Guo, A M Orsborn, et al.
Cytogenetics and Cell Genetics|January 1, 1986
A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) lociA Fratini, R N Simmers, D F Callen, et al.
Genomics|December 1, 1993
Identification and regional localization of a human IMP dehydrogenase-like locus (IMPDHL1) at 16p13.13N A Doggett, D F Callen, Z L Chen, et al.
Genomics|February 1, 1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16D F Callen, V J Hyland, E G Baker, et al.
Pageof 20