F. Schoute

Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations

C. Woods, M. Nelen, H. Kremer, 1999, European Journal of Human Genetics.

Expression of functional factor VIII in primary human skin fibroblasts after retrovirus-mediated gene transfer.

A. van der Eb, M. Verbeet, E. Briët, 1990, The Journal of biological chemistry.

Microdeletions of the Y chromosome and intracytoplasmic sperm injection: from gene to clinic.

L. Hoefsloot, D. Smeets, J. Kremer, 1997, Human reproduction.

Physiology: DAZLA: An Important Candidate Gene in Male Subfertility?

L. Hoefsloot, J. Kremer, D. Braat, 2001, Journal of Assisted Reproduction and Genetics.

Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation

M. Ligtenberg, F. Waldhauser, A. F. V. Lieburg, 1995, Human Genetics.

The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

G. Pals, B. V. van Oost, M. Ligtenberg, 1995, American Journal of Human Genetics.

Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations.

B. V. van Oost, J. Mandel, M. Ligtenberg, 1994, Biochemical and biophysical research communications.

Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.

K. Davies, S. Knight, B. Oostra, 1994, American journal of human genetics.

Identification of a two base pair deletion in five unrelated families with X-linked adrenoleukodystrophy: A possible hot spot for mutations

M. Ligtenberg, S. Kemp, P. Bolhuis, 2012 .