Smeets DF - Search Results

1

An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation.

Bodmer D, Eleveld MJ, Ligtenberg MJ, Weterman MA, Janssen BA, Smeets DF, de Wit PE, van den Berg A, van den Berg E, Koolen MI, Geurts van Kessel A. Bodmer D, et al. Among authors: smeets df. Am J Hum Genet. 1998 Jun;62(6):1475-83. doi: 10.1086/301888. Am J Hum Genet. 1998. PMID: 9585616 Free PMC article.

2

Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21).

Bodmer D, Eleveld M, Ligtenberg M, Weterman M, van der Meijden A, Koolen M, Hulsbergen-van der Kaa C, Smits A, Smeets D, Geurts van Kessel A. Bodmer D, et al. Cancer Genet Cytogenet. 2002 Apr 1;134(1):6-12. doi: 10.1016/s0165-4608(01)00585-4. Cancer Genet Cytogenet. 2002. PMID: 11996788

3

A familial case of renal cell carcinoma and a t(2;3) chromosome translocation.

Koolen MI, van der Meyden AP, Bodmer D, Eleveld M, van der Looij E, Brunner H, Smits A, van den Berg E, Smeets D, Geurts van Kessel A. Koolen MI, et al. Kidney Int. 1998 Feb;53(2):273-5. doi: 10.1046/j.1523-1755.1998.00762.x. Kidney Int. 1998. PMID: 9461085 Free article.

4

Renal cell cancer: chromosome 3 translocations as risk factors.

van Kessel AG, Wijnhoven H, Bodmer D, Eleveld M, Kiemeney L, Mulders P, Weterman M, Ligtenberg M, Smeets D, Smits A. van Kessel AG, et al. J Natl Cancer Inst. 1999 Jul 7;91(13):1159-60. doi: 10.1093/jnci/91.13.1159. J Natl Cancer Inst. 1999. PMID: 10393725 No abstract available.

5

Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15).

Eleveld MJ, Bodmer D, Merkx G, Siepman A, Sprenger SH, Weterman MA, Ligtenberg MJ, Kamp J, Stapper W, Jeuken JW, Smeets D, Smits A, Geurts Van Kessel A. Eleveld MJ, et al. Genes Chromosomes Cancer. 2001 May;31(1):23-32. doi: 10.1002/gcc.1114. Genes Chromosomes Cancer. 2001. PMID: 11284032

6

In situ detection of supernumerary aberrations of chromosome-specific repetitive DNA targets in interphase nuclei in human melanoma cell lines and tissue sections.

de Wit PE, Hopman AH, van Muijen GN, Smeets DF, Beck JL, Moesker O, Ruiter DJ. de Wit PE, et al. Among authors: smeets df. J Invest Dermatol. 1992 Apr;98(4):450-8. doi: 10.1111/1523-1747.ep12499853. J Invest Dermatol. 1992. PMID: 1548428 Free article.

7

Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas.

Forus A, Weghuis DO, Smeets D, Fodstad O, Myklebost O, Geurts van Kessel A. Forus A, et al. Genes Chromosomes Cancer. 1995 Sep;14(1):15-21. doi: 10.1002/gcc.2870140104. Genes Chromosomes Cancer. 1995. PMID: 8527379

8

Comparison of chromosome studies on PHA-stimulated blood and unstimulated bone marrow cells in recipients of lymphocyte depleted grafts using counterflow centrifugation.

Schattenberg A, Bär B, Smeets D, Geurts van Kessel A, De Witte T. Schattenberg A, et al. Bone Marrow Transplant. 1993 Feb;11(2):95-101. Bone Marrow Transplant. 1993. PMID: 8435669

9

Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.

Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Wijmenga C, et al. Among authors: smeets df. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.

10

Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH.

Veltman JA, Jonkers Y, Nuijten I, Janssen I, van der Vliet W, Huys E, Vermeesch J, Van Buggenhout G, Fryns JP, Admiraal R, Terhal P, Lacombe D, van Kessel AG, Smeets D, Schoenmakers EF, van Ravenswaaij-Arts CM. Veltman JA, et al. Am J Hum Genet. 2003 Jun;72(6):1578-84. doi: 10.1086/375695. Epub 2003 May 9. Am J Hum Genet. 2003. PMID: 12740760 Free PMC article.

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