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B Malfoy

Showing results (71-80 of 79) with videos related to

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Oncogene|July 14, 1998
GAC1, a new member of the leucine-rich repeat superfamily on chromosome band 1q32.1, is amplified and overexpressed in malignant gliomasA Almeida, X X Zhu, N Vogt, et al.
Cancer Genetics and Cytogenetics|September 1, 1997
DNA hypomethylation in breast cancer: an independent parameter of tumor progression?J Bernardino, C Roux, A Almeida, et al.
Oncogene|March 21, 2007
RB1 and TP53 pathways in radiation-induced sarcomasN Gonin-Laurent, N S Hadj-Hamou, N Vogt, et al.
Human Heredity|January 1, 1988
Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probeO Delattre, A Bernard, B Malfoy, et al.
Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.
Journal of Medical Genetics|May 16, 2002
A T to C mutation in the polypyrimidine tract of the exon 9 splicing site of the RB1 gene responsible for low penetrance hereditary retinoblastomaS H Lefévre, L Chauveinc, D Stoppa-Lyonnet, et al.
Nucleic Acids Research|October 26, 1987
Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3O Delattre, A Bernard, B Malfoy, et al.
Oncogene|January 10, 2002
Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastomaS H Lefèvre, N Vogt, A M Dutrillaux, et al.
The Journal of Molecular Diagnostics : JMD|March 29, 2001
Quantitative fluorescence in situ hybridization in lung cancer as a diagnostic markerK Truong, M Gerbault-Seureau, M N Guilly, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Oncogene|July 14, 1998
GAC1, a new member of the leucine-rich repeat superfamily on chromosome band 1q32.1, is amplified and overexpressed in malignant gliomasA Almeida, X X Zhu, N Vogt, et al.
Cancer Genetics and Cytogenetics|September 1, 1997
DNA hypomethylation in breast cancer: an independent parameter of tumor progression?J Bernardino, C Roux, A Almeida, et al.
Oncogene|March 21, 2007
RB1 and TP53 pathways in radiation-induced sarcomasN Gonin-Laurent, N S Hadj-Hamou, N Vogt, et al.
Human Heredity|January 1, 1988
Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probeO Delattre, A Bernard, B Malfoy, et al.
Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.
Journal of Medical Genetics|May 16, 2002
A T to C mutation in the polypyrimidine tract of the exon 9 splicing site of the RB1 gene responsible for low penetrance hereditary retinoblastomaS H Lefévre, L Chauveinc, D Stoppa-Lyonnet, et al.
Nucleic Acids Research|October 26, 1987
Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3O Delattre, A Bernard, B Malfoy, et al.
Oncogene|January 10, 2002
Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastomaS H Lefèvre, N Vogt, A M Dutrillaux, et al.
The Journal of Molecular Diagnostics : JMD|March 29, 2001
Quantitative fluorescence in situ hybridization in lung cancer as a diagnostic markerK Truong, M Gerbault-Seureau, M N Guilly, et al.
Pageof 8