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  1. 1998

  2. Two frequent missense mutations in Pendred syndrome

    van Hauwe, P., Everett, L. A., Coucke, P., Scott, D. A., Kraft, M. L., Ris-Stalpers, C., Bolder, C., Otten, B., de Vijlder, J. J., Dietrich, N. L., Ramesh, A., Srisailapathy, S. C., Parving, A., Cremers, C. W., Willems, P. J., Smith, R. J., Green, E. D. & van Camp, G., 1998, In: Human molecular genetics. 7, 7, p. 1099-1104

    Research output: Contribution to journal › Article › Academic › peer-review

  3. 1997

  4. Inborn errors of thyroid hormone biosynthesis

    de Vijlder, J. J., Ris-Stalpers, C. & Vulsma, T., 1997, In: Experimental and clinical endocrinology & diabetes. 105, Suppl. 4, p. 32-37

    Research output: Contribution to journal › Article › Academic › peer-review

  5. Structure, function, and relevance of thyroid peroxidase in inherited diseases of the thyroid

    De Vijlder, J. J. M., Bikker, H., Ris-Stalpers, C. & Vulsma, T., 1997, In: Current opinion in endocrinology and diabetes. 4, 5, p. 328-332 5 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  6. The revised 8307 base pair coding sequence of human thyroglobulin transiently expressed in eukaryotic cells

    van de Graaf, S. A., Pauws, E., de Vijlder, J. J. & Ris-Stalpers, C. R., 1997, In: European journal of endocrinology / European Federation of Endocrine Societies. 136, 5, p. 508-515

    Research output: Contribution to journal › Article › Academic › peer-review

  7. 1996

  8. Molecular basis of androgen insensitivity

    Brinkmann, A., Jenster, G., Ris-Stalpers, C., van der Korput, H., Brüggenwirth, H., Boehmer, A. & Trapman, J., 1996, In: Steroids. 61, 4, p. 172-175

    Research output: Contribution to journal › Article › Academic › peer-review

  9. Type II and type III deiodinase activity in human placenta as a function of gestational age

    Koopdonk-Kool, J. M., de Vijlder, J. J., Veenboer, G. J., Ris-Stalpers, C., Kok, J. H., Vulsma, T., Boer, K. & Visser, T. J., 1996, In: Journal of clinical endocrinology and metabolism. 81, 6, p. 2154-2158

    Research output: Contribution to journal › Article › Academic › peer-review

  10. 1995

  11. Androgen receptor mutations

    Brinkmann, A. O., Jenster, G., Ris-Stalpers, C., van der Korput, J. A., Brüggenwirth, H. T., Boehmer, A. L. & Trapman, J., 1995, In: Journal of steroid biochemistry and molecular biology. 53, 1-6, p. 443-448

    Research output: Contribution to journal › Article › Academic › peer-review

  12. Importance of the content and localization of tyrosine residues for thyroxine formation within the N-terminal part of human thyroglobulin

    den Hartog, M. T., Sijmons, C. C., Bakker, O., Ris-Stalpers, C. & de Vijlder, J. J., 1995, In: European journal of endocrinology / European Federation of Endocrine Societies. 132, 5, p. 611-617

    Research output: Contribution to journal › Article › Academic › peer-review

  13. 1994

  14. A practical approach to the detection of androgen receptor gene mutations and pedigree analysis in families with x-linked androgen insensitivity

    Ris-Stalpers, C., Hoogenboezem, T., Sleddens, H. F., Verleun-Mooijman, M. C., Degenhart, H. J., Drop, S. L., Halley, D. J., Oosterwijk, J. C., Hodgins, M. B. & Trapman, J., 1994, In: Pediatric research. 36, 2, p. 227-234

    Research output: Contribution to journal › Article › Academic › peer-review

  15. Differential splicing of human androgen receptor pre-mRNA in X-linked Reifenstein syndrome, because of a deletion involving a putative branch site

    Ris-Stalpers, C., Verleun-Mooijman, M. C., de Blaeij, T. J., Degenhart, H. J., Trapman, J. & Brinkmann, A. O., 1994, In: American journal of human genetics. 54, 4, p. 609-617

    Research output: Contribution to journal › Article › Academic › peer-review

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