JC Oosterwijk

Normal phenotype in two brothers with a full FMR1 mutation

H. J. M. Smeets, Anne Smits, Coleta Verheij et al. · Human Molecular Genetics · 1995 · 179 citations

Life Sciences, Genetics, Molecular Genetics +14

BRCA1 in the family: A case description of the psychological implications

A C DudokdeWit, Aad Tibben, Petra G. Frets et al. · American Journal of Medical Genetics · 1997 · 94 citations

Life Sciences, Genetics, Oncology +17

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

Monique Losekoot, E Hoogendoorn, Renske Olmer et al. · Journal of Medical Genetics · 1997 · 62 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

C. Ris-Stalpers, Theo Hoogenboezem, Hein F.B.M. Sleddens et al. · Pediatric Research · 1994 · 43 citations

Medicine, Endocrinology, Genetics +17

Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.

JC Oosterwijk, Marcel Nelen, P M van Zandvoort et al. · PubMed · 1992 · 42 citations

Life Sciences, Genetics, Molecular Genetics +7