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D F Callen

Showing results (141-150 of 195) with videos related to

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Prenatal Diagnosis|July 1, 1988
Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus samplingD F Callen, G Korban, G Dawson, et al.
American Journal of Medical Genetics|June 5, 1995
Physical map of the region containing the gene for Batten disease (CLN3)I E Järvelä, H M Mitchison, D F Callen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991
An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15P J MacKinnon, B C Powell, G E Rogers, et al.
Genes, Chromosomes & Cancer|February 1, 1994
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancerA M Cleton-Jansen, E W Moerland, N J Kuipers-Dijkshoorn, et al.
Molecular and Cellular Endocrinology|May 11, 2010
Systematic characterisation of the rat and human CYP24A1 promoterR Kumar, D N Iachini, P M Neilsen, et al.
Leukemia & Lymphoma|February 1, 1996
The biological significance of the multidrug resistance gene MRP in inversion 16 leukemiasB J Kuss, R G Deeley, S P Cole, et al.
Science (New York, N.Y.)|June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesisJ K Nancarrow, E Kremer, K Holman, et al.
Journal of Medical Genetics|February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 MbR Bell, G Brice, A H Child, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationC C Hunt, H J Eyre, P A Akkari, et al.
Genomics|February 10, 1995
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1C A Klanke, Y R Su, D F Callen, et al.
Pageof 20

Showing results (141-150 of 195) with videos related to

Sort By:
Pageof 20
Prenatal Diagnosis|July 1, 1988
Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus samplingD F Callen, G Korban, G Dawson, et al.
American Journal of Medical Genetics|June 5, 1995
Physical map of the region containing the gene for Batten disease (CLN3)I E Järvelä, H M Mitchison, D F Callen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991
An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15P J MacKinnon, B C Powell, G E Rogers, et al.
Genes, Chromosomes & Cancer|February 1, 1994
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancerA M Cleton-Jansen, E W Moerland, N J Kuipers-Dijkshoorn, et al.
Molecular and Cellular Endocrinology|May 11, 2010
Systematic characterisation of the rat and human CYP24A1 promoterR Kumar, D N Iachini, P M Neilsen, et al.
Leukemia & Lymphoma|February 1, 1996
The biological significance of the multidrug resistance gene MRP in inversion 16 leukemiasB J Kuss, R G Deeley, S P Cole, et al.
Science (New York, N.Y.)|June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesisJ K Nancarrow, E Kremer, K Holman, et al.
Journal of Medical Genetics|February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 MbR Bell, G Brice, A H Child, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationC C Hunt, H J Eyre, P A Akkari, et al.
Genomics|February 10, 1995
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1C A Klanke, Y R Su, D F Callen, et al.
Pageof 20