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A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South AfricaVAN DER MERWE, N. C; HAMEL, N; SCHNEIDER, S.-R et al.Clinical genetics. 2012, Vol 81, Num 2, pp 179-184, issn 0009-9163, 6 p.Article

Germline mutations in APC and MUTHY are responsible for the majority of families with attenuated familial adenomatous polyposisNIELSEN, M; HES, F. J; NAGENGAST, F. M et al.Clinical genetics. 2007, Vol 71, Num 5, pp 427-433, issn 0009-9163, 7 p.Article

Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomaliesBRESLAU-SIDERIUS, E. J; WIJNEN, J. T; DAUWERSE, J. G et al.Human genetics. 1993, Vol 92, Num 5, pp 481-485, issn 0340-6717Article

Distribution of adenosine deaminase-complexing protein in murine tissuesDINJENS, W. N. M; TEN KATE, J; WIJNEN, J. T et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 32, pp 19215-19220, issn 0021-9258Article

Somatic APC mosaicism : an underestimated cause of polyposis coliHES, F. J; NIELSEN, M; BIK, E. C et al.Gut. 2008, Vol 57, Num 1, issn 0017-5749, 10-12, 71-76 [9 p.]Article

Clinical findings with implications for genetic testing in families with clustering of colorectal cancerWIJNEN, J. T; VASEN, H. F. A; MEERA KHAN, P et al.The New England journal of medicine. 1998, Vol 339, Num 8, pp 511-518, issn 0028-4793Article

Mixed T-lymphoid chimerism after allogeneic bone marrow transplantatin for hematologic malignancies of children is not correlated with relapseVAN LEEUWEN, J. E. M; VAN TOL, M. J. D; JOOSTEN, A. M et al.Blood. 1993, Vol 82, Num 6, pp 1921-1928, issn 0006-4971Article

Structure of the bovine eye lens γs-crystallin gene (formerly βs)VAN RENS, G. L. M; RAATS, J. M. H; DRIESSEN, H. P. C et al.Gene (Amsterdam). 1989, Vol 78, Num 2, pp 225-233, issn 0378-1119Article

Prevalence and molecular heterogeneity of alpha+ thalassemia in two tribal populations from Andhra Pradesh, IndiaFODDE, R; LOSEKOOT, M; BERNINI, L. F et al.Human genetics. 1988, Vol 80, Num 2, pp 157-160, issn 0340-6717Article

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutationWAGNER, A; TOPS, C; MEIJERS-HEIJBOER, H et al.Journal of medical genetics. 2002, Vol 39, Num 11, pp 833-837, issn 0022-2593, 5 p.Article

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers : A study of hereditary nonpolyposis colorectal cancer familiesVASEN, H. F. A; STORMORKEN, A; MENKO, F. H et al.Journal of clinical oncology. 2001, Vol 19, Num 20, pp 4074-4080, issn 0732-183XArticle

Gene-environment interaction in hereditary nonpolyposis colorectal cancer with implications for diagnosis and genetic testingPARK, J.-G; PARK, Y. J; WIJNEN, J. T et al.International journal of cancer. 1999, Vol 82, Num 4, pp 516-519, issn 0020-7136Article

Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infectionsROOS, D; VAN ZWIETEN, R; VULLIAMY, T. J et al.Blood. 1999, Vol 94, Num 9, pp 2955-2962, issn 0006-4971Article

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli : implications for presymptomatic diagnosisTOPS, C. M. J; BREUKEL, C; MEERA KHAN, P et al.Human genetics. 1991, Vol 86, Num 4, pp 365-368, issn 0340-6717Article

Distribution of adenosine deaminase complexing protein (ADCP) in human tissuesDINJENS, W. N. M; TEN KATE, J; VAN DER LINDEN, E. P. M et al.The Journal of histochemistry and cytochemistry. 1989, Vol 37, Num 12, pp 1869-1875, issn 0022-1554Article

Childhood brain tumours due to germline bi-allelic mismatch repair gene mutationsJOHANNESMA, P. C; DER KLIFT, Hm Van; MENKO, F. H et al.Clinical genetics. 2011, Vol 80, Num 3, pp 243-255, issn 0009-9163, 13 p.Article

Peutz—Jeghers syndrome: a systematic review and recommendations for managementBEGGS, A. D; LATCHFORD, A. R; CAPELLA, G et al.Gut. 2010, Vol 59, Num 7, pp 975-986, issn 0017-5749, 12 p.Article

Preemptive alloimmune intervention in high-risk pediatric acute lymphoblastic leukemia patients guided by minimal residual disease level before stem cell transplantationLANKESTER, A. C; BIERINGS, M. B; PUTTER, H et al.Leukemia. 2010, Vol 24, Num 8, pp 1462-1469, issn 0887-6924, 8 p.Article

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA I and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCAI/BRCA2 (CIMBA)OSORIO, A; MILNE, R. L; HEALEY, S et al.British journal of cancer. 2009, Vol 101, Num 12, pp 2048-2054, issn 0007-0920, 7 p.Article

Suspected hereditary nonpolyposis colorectal cancer : International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosisPARK, J.-G; VASEN, H. F. A; WIJNEN, J. T et al.Diseases of the colon & rectum. 1999, Vol 42, Num 6, pp 710-716, issn 0012-3706Article

Persistence of host-type hematopoiesis after allogeneic bone marrow transplantation for leukemia is significantly related to the recipient's age and/or the conditioning regimen, but it is not associated with an increased risk of relapseVAN LEEUWEN, J. E. M; VAN TOL, M. J. D; JOOSTEN, A. M et al.Blood. 1994, Vol 83, Num 10, pp 3059-3067, issn 0006-4971Article

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancerTOMLINSON, Ipm; DUNLOP, M; AALTONEN, L. A et al.British journal of cancer. 2010, Vol 102, Num 2, pp 447-454, issn 0007-0920, 8 p.Article

Human αB-crystallin (CRYA2)gene mapped to chromosome 11q12-q23BRAKENHOFF, R. H; GEURTS, A. H. M; OLDENBURG, M et al.Human genetics. 1990, Vol 85, Num 2, pp 237-240, issn 0340-6717Article

Presymptomatic diagnosis of familial adenomatous polyposis by bridging DNA markersTOPS, C. M. J; GRIFFIOEN, G; MEERA KHAN, P et al.Lancet (British edition). 1989, Vol 2, Num 8676, pp 1361-1363, issn 0140-6736, 3 p.Article

Assignment of the human tissue-type plasminogen activator gene (PLAT) to chromosome PVERHEIJEN, J. H; VISSE, R; WIJNEN, J. T et al.Human genetics. 1986, Vol 72, Num 2, pp 153-156, issn 0340-6717Article

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