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N Mandahl

Showing results (121-130 of 336) with videos related to

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Cancer Genetics and Cytogenetics|November 1, 1992
Trisomy 7 in nonneoplastic kidney tissue cultured with and without epidermal growth factorP Elfving, R Lundgren, J C Cigudosa, et al.
Cancer Genetics and Cytogenetics|June 1, 1988
t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinomaY S Jin, N Mandahl, S Heim, et al.
Cancer Genetics and Cytogenetics|September 2, 1998
Cytogenetic heterogeneity in a second primary radiation-induced bladder carcinoma: ten karyotypically unrelated clonesI Fadl-Elmula, L Bonaldi, L Gorunova, et al.
Cancer Genetics and Cytogenetics|May 1, 1990
Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovaryT Pejovic, S Heim, N Mandahl, et al.
Cancer Genetics and Cytogenetics|January 1, 1988
Unique karyotypic abnormalities in a squamous cell carcinoma of the larynxY S Jin, N Mandahl, S Heim, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Chromosome abnormalities in a pancreatic adenocarcinomaB Johansson, N Mandahl, S Heim, et al.
International Journal of Cancer|August 9, 1995
Translocation t(9;22)(q22;q12) is a primary cytogenetic abnormality in extraskeletal myxoid chondrosarcomaG Stenman, H Andersson, N Mandahl, et al.
Human Genetics|October 1, 1990
Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomasM Nilbert, S Heim, N Mandahl, et al.
Cytogenetics and Cell Genetics|February 2, 1999
Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritisK Broberg, M Höglund, A Lindstrand, et al.
Acta Orthopaedica Scandinavica|October 1, 1988
A case of Ewing's sarcoma diagnosed by fine needle aspiration. Light microscopy, electron microscopy and chromosomal analysisM Akerman, T Alvegård, J Eliasson, et al.
Pageof 34

Showing results (121-130 of 336) with videos related to

Sort By:
Pageof 34
Cancer Genetics and Cytogenetics|November 1, 1992
Trisomy 7 in nonneoplastic kidney tissue cultured with and without epidermal growth factorP Elfving, R Lundgren, J C Cigudosa, et al.
Cancer Genetics and Cytogenetics|June 1, 1988
t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinomaY S Jin, N Mandahl, S Heim, et al.
Cancer Genetics and Cytogenetics|September 2, 1998
Cytogenetic heterogeneity in a second primary radiation-induced bladder carcinoma: ten karyotypically unrelated clonesI Fadl-Elmula, L Bonaldi, L Gorunova, et al.
Cancer Genetics and Cytogenetics|May 1, 1990
Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovaryT Pejovic, S Heim, N Mandahl, et al.
Cancer Genetics and Cytogenetics|January 1, 1988
Unique karyotypic abnormalities in a squamous cell carcinoma of the larynxY S Jin, N Mandahl, S Heim, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Chromosome abnormalities in a pancreatic adenocarcinomaB Johansson, N Mandahl, S Heim, et al.
International Journal of Cancer|August 9, 1995
Translocation t(9;22)(q22;q12) is a primary cytogenetic abnormality in extraskeletal myxoid chondrosarcomaG Stenman, H Andersson, N Mandahl, et al.
Human Genetics|October 1, 1990
Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomasM Nilbert, S Heim, N Mandahl, et al.
Cytogenetics and Cell Genetics|February 2, 1999
Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritisK Broberg, M Höglund, A Lindstrand, et al.
Acta Orthopaedica Scandinavica|October 1, 1988
A case of Ewing's sarcoma diagnosed by fine needle aspiration. Light microscopy, electron microscopy and chromosomal analysisM Akerman, T Alvegård, J Eliasson, et al.
Pageof 34