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10 Most Recent Publications
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Concluding remarks: "Biobanking for cancer research: Rules and roles," november 2010, Bari, Italy
(Article)
Riegman, P.H.J. Daidone, M.G. Paradiso, A. |
2011-06-01
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Semi-automatic identification of punching areas for tissue microarray building: The tubular breast cancer pilot study
(Article)
Viti, F. Merelli, I. Timmermans, A.M. Bakker, M.A. den Beltrame, F. Riegman, P.H.J. Milanesi, L. |
2010-11-18
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What are three actionable strategies to improve quality in biomedical research
(Article)
Vaught, J. Baust, J.G. Heacox, A.E. Riegman, P.H.J. Betsou, F. Mazur, P. Stacey, G. Barnes, M. |
2010-09-01
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Towards norms for accreditation of biobanks for human health and medical research: Compilation of existing guidelines into an ISO certification/accreditation norm-compatible format
(Article)
Betsou, F. Luzergues, A. Carter, A. Geary, P. Riegman, P.H.J. Clark, B. Morente, M.M. Vaught, J. Dhirr, R. Druez-Vérité, C. |
2007-12-01
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Standard operating procedure for the collection of fresh frozen tissue samples
(Article)
Mager, S.R. Oomen, M.H.A. Morente, M.M. Ratcliffe, C. Knox, K. Kerr, D. Pezzella, F. Riegman, P.H.J. |
2007-03-01
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Targeted disruption of the Mn1 oncogene results in severe defects in development of membranous bones of the cranial skeleton.
(Article)
Meester-Smoor, M.A. Vermeij, M. Helmond, M.J. van Molijn, A.C. Wely, K.H. van Hekman, A.C. Vermey-Keers, C. Riegman, P.H.J. Zwarthoff, E.C. |
2005-05-01
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Allelic imbalance of 7q32.3-q36.1 during tumorigenesis in Barrett's esophagus
(Article)
Riegman, P.H.J. Burgart, L.J. Wang, K.K. Wink-Godschalk, J.C. Dinjens, W.N.M. Siersema, P.D. Tilanus, H.W. Dekken, H. van |
2002-01-01
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Genomic alterations in malignant transformation of Barrett's esophagus
(Article)
Riegman, P.H.J. Vissers, K.J. Alers, J.C. Geelen, E. Hop, W.C.J. Tilanus, H.W. Dekken, H. van |
2001-01-01
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Molecular cytogenetic evaluation of gastric cardia adenocarcinoma and precursor lesions
(Article)
Dekken, H. van Alers, J.C. Riegman, P.H.J. Rosenberg, C. Tilanus, H.W. Vissers, K. |
2001-01-01
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A G-->A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2
(Article)
Klein, J.E.M.M. de Riegman, P.H.J. Bijlsma, E.K. Heldoorn, A. Muijtjens, M. Bakker, M.A. den Avezaat, C.J.J. Zwarthoff, E.C. |
1998-01-01
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