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D F Callen

Showing results (51-60 of 195) with videos related to

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Cancer Genetics and Cytogenetics|March 1, 1988
Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3A H Puspurs, E Baker, D F Callen, et al.
Clinical Genetics|November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boyS Schuffenhauer, D F Callen, H Seidel, et al.
Genomics|September 1, 1994
Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2I A Aksoy, D F Callen, S Apostolou, et al.
Genomics|August 1, 1991
Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sitesR I Richards, K Holman, S Lane, et al.
Journal of Human Genetics|November 26, 1999
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainK Bhalla, H J Eyre, S A Whitmore, et al.
Genomics|June 6, 1998
Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosityG Kremmidiotis, E Baker, J Crawford, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24M A Pritchard, E Baker, D F Callen, et al.
Clinical Genetics|June 1, 1994
Discordance between direct and PHA-stimulated chromosome preparations from neonatesI W Garnham, H Fernandez, D F Callen, et al.
Nucleic Acids Research|September 26, 1988
ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1A Fratini, E G Baker, D F Callen, et al.
Nucleic Acids Research|September 26, 1988
RsaI and TaqI RFLPs for pACHF3.5 [D16S10]A Fratini, E G Baker, D F Callen, et al.
Pageof 20

Showing results (51-60 of 195) with videos related to

Sort By:
Pageof 20
Cancer Genetics and Cytogenetics|March 1, 1988
Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3A H Puspurs, E Baker, D F Callen, et al.
Clinical Genetics|November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boyS Schuffenhauer, D F Callen, H Seidel, et al.
Genomics|September 1, 1994
Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2I A Aksoy, D F Callen, S Apostolou, et al.
Genomics|August 1, 1991
Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sitesR I Richards, K Holman, S Lane, et al.
Journal of Human Genetics|November 26, 1999
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainK Bhalla, H J Eyre, S A Whitmore, et al.
Genomics|June 6, 1998
Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosityG Kremmidiotis, E Baker, J Crawford, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24M A Pritchard, E Baker, D F Callen, et al.
Clinical Genetics|June 1, 1994
Discordance between direct and PHA-stimulated chromosome preparations from neonatesI W Garnham, H Fernandez, D F Callen, et al.
Nucleic Acids Research|September 26, 1988
ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1A Fratini, E G Baker, D F Callen, et al.
Nucleic Acids Research|September 26, 1988
RsaI and TaqI RFLPs for pACHF3.5 [D16S10]A Fratini, E G Baker, D F Callen, et al.
Pageof 20