A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testingDØRUM, A; MØLLER, P; VAN DER MEULEN, M. A et al.European journal of cancer (1990). 1997, Vol 33, Num 14, pp 2390-2392, issn 0959-8049Article

Early-onset renal cell cancer and bilateral epididymal cysts as presenting symptoms of von Hippel-Lindau diseaseKROES, H. Y; SIJMONS, R. H; VAN DEN BERG, A et al.British journal of urology (Print). 1998, Vol 81, Num 6, issn 0007-1331, p. 915Article

Optimal selection for BRCA I and BRCA2 mutation testing using a combination of 'easy to apply' probability modelsBODMER, D; LIGTENBERG, M. J. L; VAN DER HOUT, A. H et al.British journal of cancer. 2006, Vol 95, Num 6, pp 757-762, issn 0007-0920, 6 p.Article

Localization by in situ hybridization of three 3p probes with respect to the breakpoint in a t(3;8) in hereditary renal cell carcinomaVAN DER HOUT, A. H; BROWN, R. S; LI, F. P et al.Cancer genetics and cytogenetics. 1991, Vol 51, Num 1, pp 121-124, issn 0165-4608, 4 p.Article

Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletionVAN DER HOUT, A. H; VAN DER VEEN, A. Y; ATEN, J. A et al.Human genetics. 1988, Vol 80, Num 2, pp 161-164, issn 0340-6717Article

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer familiesPEELEN, T; VAN VLIET, M; VAN DER LUIJT, R et al.American journal of human genetics. 1997, Vol 60, Num 5, pp 1041-1049, issn 0002-9297Article

A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomesKOK, K; VAN DEN BERG, A; BUYS, C. H. C. M et al.Cancer research (Baltimore). 1994, Vol 54, Num 15, pp 4183-4187, issn 0008-5472Article

Translocation (11;22)(q24;q12) in a small cell tumor of the thigh in a 2-year-old boy : Immunohistology, cytogenetics, molecular genetics, and review of the literatureMASTIK, M. F; MOLENAAR, W. M; PLAAT, B. E. C et al.Human pathology. 1999, Vol 30, Num 3, pp 352-355, issn 0046-8177Article

A single Na⁺ channel mutation causing both long-QT and Brugada syndromesBEZZINA, C; VELDKAMP, M. W; MANNENS, M. M. A. M et al.Circulation research. 1999, Vol 85, Num 12, pp 1206-1213, issn 0009-7330Article

Loss of heterozygosity at the short arm of chromosome 3 in renal-cell cancer correlates with the cytological tumour typeVAN DER HOUT, A. H; VAN DEN BERG, E; VAN DER VLIES, P et al.International journal of cancer. 1993, Vol 53, Num 3, pp 353-357, issn 0020-7136Article

The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy : an updated protocolVAN ESSEN, A. J; KNEPPERS, A. L. J; VAN DER HOUT, A. H et al.Journal of medical genetics. 1997, Vol 34, Num 10, pp 805-812, issn 0022-2593Article

Construction of a pulsed-field amp around D3S3 using partially demethylated DNAVAN DER HOUT, A. H; HULSBEEK, M. M. F; BUYS, C. H. C. M et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 134-137, issn 0301-0171Conference Paper

The region of common allelic losses in sporadic renal cell carcinoma is bordered by the loci D3C2 and THRBVAN DER HOUT, A. H; VAN DER VLIES, P; WIJMENGA, C et al.Genomics (San Diego, Calif.). 1991, Vol 11, Num 3, pp 537-542, issn 0888-7543Article

SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALSVELDINK, J. H; KALMIJN, S; VAN DER HOUT, A. H et al.Neurology. 2005, Vol 65, Num 6, pp 820-825, issn 0028-3878, 6 p.Article

BRCA1 and BRCA2 heterozygosity and repair of X-ray-induced DNA damageNIEUWENHUIS, B; VAN ASSEN-BOLT, A. J; VAN WAARDE-VERHAGEN, M. A. W. H et al.International journal of radiation biology (Print). 2002, Vol 78, Num 4, pp 285-295, issn 0955-3002Article

Cytogenetic analysis of epithelial renal-cell tumors : relationship with a new histopathological classificationVAN DEN BERG, E; VAN DER HOUT, A. H; OOSTERHUIS, J. W et al.International journal of cancer. 1993, Vol 55, Num 2, pp 223-227, issn 0020-7136Article

Localization of amplified c-myc and n-myc in small cell lung cancer cell linesVAN DER HOUT, A. H; KOK, K; VAN DER VEEN, A. Y et al.Cancer genetics and cytogenetics. 1989, Vol 38, Num 1, pp 1-8, issn 0165-4608Article

A straightforward to isolate DNA sequences with potential linkage to the retinoblastoma locusSCHEFFER, H; VAN DER LELIE, D; AANSTOOT, G. H et al.Human genetics. 1986, Vol 74, Num 3, pp 249-255, issn 0340-6717Article

Direct molecular analysis of a deletion of 3 p in tumors from patients with sporadic renal cell carcinomaVAN DER HOUT, A. H; KOK, K; VAN DER BERG, A et al.Cancer genetics and cytogenetics. 1988, Vol 32, Num 2, pp 281-285, issn 0165-4608Article

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancerKOK, K; OSINGA, J; POPPEMA, S et al.Nature (London). 1987, Vol 330, Num 6148, pp 578-581, issn 0028-0836Article

Characterization and chromosomal assignment of yeast artificial chromosomes containing human 3p13-p21-specific sequence tagged sitesMICHAELIS, S. C; BARDENHEUER, W; BUYS, C. H. C. M et al.Cancer genetics and cytogenetics. 1995, Vol 81, Num 1, pp 1-12, issn 0165-4608Article