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B K Hecht

Showing results (91-100 of 106) with videos related to

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Cancer Genetics and Cytogenetics|March 1, 1988
Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14E H Tajara, C S Berger, B K Hecht, et al.
Clinical Genetics|June 1, 1993
Direct molecular diagnosis of myotonic dystrophyB K Hecht, A Donnelly, A K Gedeon, et al.
Journal of Medical Genetics|November 1, 1988
Chromosome subband 17p11.2 deletion: a minute deletion syndromeD Lockwood, F Hecht, C Dowman, et al.
Cancer Genetics and Cytogenetics|October 1, 1995
Cytogenetics of malignant gliomas: I. The autosomes with reference to rearrangementsB K Hecht, C Turc-Carel, M Chatel, et al.
Cancer Genetics and Cytogenetics|October 1, 1995
Cytogenetics of malignant gliomas. II. The sex chromosomes with reference to X isodisomy and the role of numerical X/Y changesB K Hecht, C Turc-Carel, M Chatel, et al.
Cancer|February 1, 1992
X;6 translocation in a child with congenital acute lymphocytic leukemiaL A Carney, J S Kinney, R R Higgins, et al.
Blood|June 1, 1989
Lack of involvement of the c-fms and N-myc genes by chromosomal translocation t(2;5)(p23;q35) common to malignancies with features of so-called malignant histiocytosisR Morgan, S D Smith, B K Hecht, et al.
Cancer Genetics and Cytogenetics|March 1, 1988
Fragile sites and genitourinary tumorsE H Tajara, B K Hecht, D Lockwood, et al.
Cancer Genetics and Cytogenetics|January 1, 1984
Direct prenatal chromosome diagnosis of a malignancyF Hecht, A Grix, B K Hecht, et al.
Oncogene Research|May 1, 1988
Chromosomal localization of the human genes for lipocortin I and lipocortin IIK Huebner, L A Cannizzaro, A Z Frey, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Cancer Genetics and Cytogenetics|March 1, 1988
Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14E H Tajara, C S Berger, B K Hecht, et al.
Clinical Genetics|June 1, 1993
Direct molecular diagnosis of myotonic dystrophyB K Hecht, A Donnelly, A K Gedeon, et al.
Journal of Medical Genetics|November 1, 1988
Chromosome subband 17p11.2 deletion: a minute deletion syndromeD Lockwood, F Hecht, C Dowman, et al.
Cancer Genetics and Cytogenetics|October 1, 1995
Cytogenetics of malignant gliomas: I. The autosomes with reference to rearrangementsB K Hecht, C Turc-Carel, M Chatel, et al.
Cancer Genetics and Cytogenetics|October 1, 1995
Cytogenetics of malignant gliomas. II. The sex chromosomes with reference to X isodisomy and the role of numerical X/Y changesB K Hecht, C Turc-Carel, M Chatel, et al.
Cancer|February 1, 1992
X;6 translocation in a child with congenital acute lymphocytic leukemiaL A Carney, J S Kinney, R R Higgins, et al.
Blood|June 1, 1989
Lack of involvement of the c-fms and N-myc genes by chromosomal translocation t(2;5)(p23;q35) common to malignancies with features of so-called malignant histiocytosisR Morgan, S D Smith, B K Hecht, et al.
Cancer Genetics and Cytogenetics|March 1, 1988
Fragile sites and genitourinary tumorsE H Tajara, B K Hecht, D Lockwood, et al.
Cancer Genetics and Cytogenetics|January 1, 1984
Direct prenatal chromosome diagnosis of a malignancyF Hecht, A Grix, B K Hecht, et al.
Oncogene Research|May 1, 1988
Chromosomal localization of the human genes for lipocortin I and lipocortin IIK Huebner, L A Cannizzaro, A Z Frey, et al.
Pageof 11