PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy von van der Steege, G., Grootscholten, P.M., van der Vlies, P., Draaijers, T.G., Osinga, J., Cobben, J.M., Scheffer, H., Buys, C.H.C.M.

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Predictive value of thymidylate synthase and dihydropyrimidine dehydrogenase protein expression on survival in adjuvantly treated stage III colon cancer patients von Westra, J. L., Hollema, H., Schaapveld, M., Platteel, I., Oien, K. A., Keith, W. N., Mauritz, R., Peters, G. J., Buys, C. H. C. M., Hofstra, R. M. W., Plukker, J. Th. M.

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Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11–q21 von Troelstra, C., Landsvater, R.M., Wiegant, J., van der Ploeg, M., Viel, G., Buys, C.H.C.M., Hoeijmakers, J.H.J.

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N.P.2 04 Patients with spinal muscular atrophy (SMA) and healthy siblings sharing homozygous deletions of the SMN1 gene reveal an identical number of SMN2 gene copies but different... von Lemmink, H.H., Vos, Y.J., Plaza de Menacho, I., Dijkhuis, J., Knoers, N.V.A.M., de Visser, M., Buys, C.H.C.M.

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Novel expressed sequences obtained by means of a suppression subtractive hybridisation analysis from the 6q21 region that is frequently deleted in gastric cancer von Carvalho, B., Seruca, R., Buys, C.H.C.M., Kok, K.

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Cystic fibrosis allele segregation von TEN KATE, L. P, TE MEERMAN, G. J, BUYS, C.H.C.M, HALLEY, D.J.J, OOSTRA, B

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RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia von van Everdink, W.J, Baranova, A, Lummen, C, Tyazhelova, T, Looman, M.W.G, Ivanov, D, Verlind, E, Pestova, A, Faber, H, van der Veen, A.Y, Yankovsky, N, Vellenga, E, Buys, C.H.C.M

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Dukes'C colon cancer after adjuvant treatment: can KRAS and PT 53 mutations serve as prognostic indicators? von Bleeker, W.A., Hayes, V.M., Karrenbeld, A., Hofstra, R.M.W., Verlind, E., Hermans, J., Poppema, S., Buys, C.H.C.M., Plukker, J.Th.M.

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Chimeric RNA-DNA oligonucleotide mediated gene correction of a COLI7A1 mutation in keratinocytes of a GABEB patient von van der Steege, G., Nijenhuis, M., Heeres, K., Pas, H.H., Buys, C.H.C.M., Scheffer, H., Jonkman, M.F.

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Coexistent Hirschsprung's disease and esophageal achalasia in male siblings von Kelly, J.L, Mulcahy, T.M, O'Riordain, D.S, Buys, C.H.C.M, Hofstra, R.M.W, McCarthy, T, Kirwan, W.O

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S3.2. Experience with DGGE based mutation screening of the CFTR gene in CF and CBAVD patients von Scheffer, H., de Jong, D., Mol, G.J.J., Wu, Y., Hofstra, R.M.W., Buys, C.H.C.M.

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A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing von Dørum, A, Møller, P, Kamsteeg, E.J, Scheffer, H, Burton, M, Heimdal, K.R, Mæhle, L.O, Hovig, E, Tropé, C.G, van der Hout, A.H, van der Meulen, M.A, Buys, C.H.C.M, te Meerman, G.J

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Prenatal Prediction of Spinal Muscular Atrophy von Chobben, J.M., Scheffer, H., De Visser, M., Van der Steege, G., Verhey, J.B.B.M., Osinga, J., Burton, M., Mensink, R.G.J., Grootscholten, P.M., Ten Kate, L.P., Buys, C.H.C.M.

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A highly informative dinucleotide repeat polymorphism at D13S201, between RB1 and WND von KOOY, R. F, VERLIND, E, WIJNGAARD, A, SHAPIRO, D. N, SCHEFFER, H, BUYS, C. H. C. M

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Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10 von Landsvater, R.M., Mathew, C.G.P., Smith, B.A., Marcus, E.M., te Meerman, G.J., Lips, C.J.M., Geerdink, R.A., Nakamura, Y., Ponder, B.A.J., Buys, C.H.C.M.

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The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with Sspl von Bowcock, A.M., Hebert, J.M., Scheffer, H., Penninga, D., Buys, C.H.C.M.

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The single copy probe pG24E2.4 [D13S21] reveals a Bspl286 RFLP at 13ql4.1–ql4.2 von Bowcock, A.M., Hebert, J.M., Scheffer, H., Penninga, D., Buys, C.H.C.M.

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An anonymous single copy genomic clone at 13q12–13q13 identifies three RFLPs [HGM8] assignment no. D13S11 von Scheffer, H., Penninga, D., Goor, N., Pearson, P. L., Buys, C.H.C.M.

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IDENTIFICATION OF CROSSOVERS IN WILSON DISEASE FAMILIES AS REFERENCE POINTS FOR A GENETIC LOCALIZATION OF THE GENE von SCHEFFER, H, HOUWEN, RHJ, TEMEERMAN, GJ, LOESSNER, J, BACHMANN, B, KUNERT, E, VERLIND, E, BUYS, CHCM

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A new RFLP identified at the D3S48 locus von KOK, K, FAN, M.-Z, JONAS, A, VAN DEN BERG, A, CARRITT, B, BUYS, C. H. C. M

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