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H J Decker

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Cancer Genetics and Cytogenetics|January 1, 1991
Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probesM Kiechle-Schwarz, H J Decker, C S Berger, et al.
Human Genetics|May 1, 1989
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndromeM Kiechle-Schwarz, H P Neumann, H J Decker, et al.
Oncogene|July 3, 1997
The FHIT gene is alternatively spliced in normal kidney and renal cell carcinomaX Luan, G Shi, M Zohouri, et al.
British Journal of Cancer|September 5, 2001
Frequent genomic imbalances suggest commonly altered tumour genes in human hepatocarcinogenesisF Niketeghad, H J Decker, W H Caselmann, et al.
Cancer Research|November 26, 1997
Loss of heterozygosity studies and deletion mapping identify two putative chromosome 14q tumor suppressor loci in renal oncocytomasR F Schwerdtle, A Winterpacht, S Störkel, et al.
Cancer Genetics and Cytogenetics|August 1, 1989
inv(12)(p11.2q13) in an endometrial polypT A Walter, S X Fan, M T Medchill, et al.
Cancer Genetics and Cytogenetics|April 1, 1997
Involvement of the chromosomal region 11q13 in renal oncocytoma: case report and literature reviewC Neuhaus, T Dijkhuizen, E van den Berg, et al.
Human Genetics|August 1, 1990
Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization studyH J Decker, L A Cannizzaro, M J Mendez, et al.
Cancer Genetics and Cytogenetics|March 4, 2000
Autologous transplantation of in vivo purged PBSC in CML: comparison of FISH, cytogenetics, and PCR detection of Philadelphia chromosome in leukapheresis productsG Hess, C Reifenrath, A Friedrich-Freksa, et al.
Cancer Research|July 1, 1996
Allelic losses at chromosomes 1p, 2p, 6p, 10p, 13q, 17p, and 21q significantly correlate with the chromophobe subtype of renal cell carcinomaR F Schwerdtle, S Störkel, C Neuhaus, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|January 1, 1991
Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probesM Kiechle-Schwarz, H J Decker, C S Berger, et al.
Human Genetics|May 1, 1989
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndromeM Kiechle-Schwarz, H P Neumann, H J Decker, et al.
Oncogene|July 3, 1997
The FHIT gene is alternatively spliced in normal kidney and renal cell carcinomaX Luan, G Shi, M Zohouri, et al.
British Journal of Cancer|September 5, 2001
Frequent genomic imbalances suggest commonly altered tumour genes in human hepatocarcinogenesisF Niketeghad, H J Decker, W H Caselmann, et al.
Cancer Research|November 26, 1997
Loss of heterozygosity studies and deletion mapping identify two putative chromosome 14q tumor suppressor loci in renal oncocytomasR F Schwerdtle, A Winterpacht, S Störkel, et al.
Cancer Genetics and Cytogenetics|August 1, 1989
inv(12)(p11.2q13) in an endometrial polypT A Walter, S X Fan, M T Medchill, et al.
Cancer Genetics and Cytogenetics|April 1, 1997
Involvement of the chromosomal region 11q13 in renal oncocytoma: case report and literature reviewC Neuhaus, T Dijkhuizen, E van den Berg, et al.
Human Genetics|August 1, 1990
Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization studyH J Decker, L A Cannizzaro, M J Mendez, et al.
Cancer Genetics and Cytogenetics|March 4, 2000
Autologous transplantation of in vivo purged PBSC in CML: comparison of FISH, cytogenetics, and PCR detection of Philadelphia chromosome in leukapheresis productsG Hess, C Reifenrath, A Friedrich-Freksa, et al.
Cancer Research|July 1, 1996
Allelic losses at chromosomes 1p, 2p, 6p, 10p, 13q, 17p, and 21q significantly correlate with the chromophobe subtype of renal cell carcinomaR F Schwerdtle, S Störkel, C Neuhaus, et al.
Pageof 3