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F Arwert

Showing results (41-50 of 73) with videos related to

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Genes, Chromosomes & Cancer|January 1, 1996
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinomaM A Hermsen, H Joenje, F Arwert, et al.
Familial Cancer|October 24, 2003
Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemiaM A Hermsen, Y Xie, M A Rooimans, et al.
Biochemical Genetics|February 1, 1985
Localization of the gene for the vitamin B12 binding protein, transcobalamin II, near the centromere on mouse chromosome 11, linked with the hemoglobin alpha-chain locusM Fràter-Schröder, M Prochazka, O Haller, et al.
Genomics|July 1, 1989
The human alpha-amylase multigene family consists of haplotypes with variable numbers of genesP C Groot, M J Bleeker, J C Pronk, et al.
Cancer Research|June 1, 1996
Inheritance of abnormal expression of SOS-like response in xeroderma pigmentosum and hereditary cancer-prone syndromesP J Abrahams, A Houweling, D M Cornelissen-Steijger, et al.
Clinical Genetics|March 1, 1986
The Cowden syndrome: a clinical and genetic study in 21 patientsT M Starink, J P van der Veen, F Arwert, et al.
Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.
Genomics|September 1, 1990
Evolution of the human alpha-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossoversP C Groot, W H Mager, N V Henriquez, et al.
American Journal of Medical Genetics|January 31, 1997
An atypical case of Fanconi anemia in elderly sibsM L Kwee, J M van der Kleij, A J van Essen, et al.
Journal of the National Cancer Institute|July 7, 1999
Inherited susceptibility to bleomycin-induced chromatid breaks in cultured peripheral blood lymphocytesJ Cloos, E J Nieuwenhuis, D I Boomsma, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Genes, Chromosomes & Cancer|January 1, 1996
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinomaM A Hermsen, H Joenje, F Arwert, et al.
Familial Cancer|October 24, 2003
Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemiaM A Hermsen, Y Xie, M A Rooimans, et al.
Biochemical Genetics|February 1, 1985
Localization of the gene for the vitamin B12 binding protein, transcobalamin II, near the centromere on mouse chromosome 11, linked with the hemoglobin alpha-chain locusM Fràter-Schröder, M Prochazka, O Haller, et al.
Genomics|July 1, 1989
The human alpha-amylase multigene family consists of haplotypes with variable numbers of genesP C Groot, M J Bleeker, J C Pronk, et al.
Cancer Research|June 1, 1996
Inheritance of abnormal expression of SOS-like response in xeroderma pigmentosum and hereditary cancer-prone syndromesP J Abrahams, A Houweling, D M Cornelissen-Steijger, et al.
Clinical Genetics|March 1, 1986
The Cowden syndrome: a clinical and genetic study in 21 patientsT M Starink, J P van der Veen, F Arwert, et al.
Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.
Genomics|September 1, 1990
Evolution of the human alpha-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossoversP C Groot, W H Mager, N V Henriquez, et al.
American Journal of Medical Genetics|January 31, 1997
An atypical case of Fanconi anemia in elderly sibsM L Kwee, J M van der Kleij, A J van Essen, et al.
Journal of the National Cancer Institute|July 7, 1999
Inherited susceptibility to bleomycin-induced chromatid breaks in cultured peripheral blood lymphocytesJ Cloos, E J Nieuwenhuis, D I Boomsma, et al.
Pageof 8