C. van der Sijs‐Bos

De novo recurrent germline mutation of theBRCA2 gene in a patient with early onset breast cancer

M. Ausems, R. B. van der Luijt, C. Wárlám-Rodenhuis, 2001, Journal of medical genetics.

Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.

J. Derks, J. Engelen, J. de Pater, 2006, European journal of medical genetics.

MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME 22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY 22

P. Stoutenbeek, G. Christiaens, N. Leschot, 1997, Prenatal diagnosis.

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

J. Engelen, L. Govaerts, G. Christiaens, 2003, Prenatal diagnosis.