M. Verleun-Mooijman

Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations

W. F. Abdo, K. Leenders, L. Lopiano, 2011, neurogenetics.

Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability.

A. Brinkmann, S. Drop, M. Niermeijer, 2001, The Journal of clinical endocrinology and metabolism.

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

J. Trapman, C. Ris-Stalpers, A. Brinkmann, 1994, American journal of human genetics.

Androgen receptor status in localized and locally progressive hormone refractory human prostate cancer.

Schr, T. H. van der Kwast, F. Schröder, 1994, The American journal of pathology.

Genotype versus phenotype in families with androgen insensitivity syndrome.

W J Kleijer, T. H. van der Kwast, H. Brunner, 2001, The Journal of clinical endocrinology and metabolism.

Molecular analysis of the androgen-receptor gene in a family with receptor-positive partial androgen insensitivity: an unusual type of intronic mutation.

J. Trapman, J. Grootegoed, A. Brinkmann, 1997, American journal of human genetics.

Molecular basis of androgen insensitivity

J. Trapman, A. Brinkmann, W. Kleijer, 1996, The Journal of Steroid Biochemistry and Molecular Biology.

A Practical Approach to the Detection of Androgen Receptor Gene Mutations and Pedigree Analysis in Families with X-Linked Androgen Insensitivity

J. Oosterwijk, J. Trapman, D. Halley, 1994, Pediatric Research.

Molecular basis of androgen insensitivity

J. Trapman, A. Brinkmann, H. Brüggenwirth, 1996, The Journal of Steroid Biochemistry and Molecular Biology.