F. Vries

Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies

R. Galjaard, M. Srebniak, M. Joosten, 2015, Human mutation.

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs

M. Knapen, J. Knijnenburg, R. Galjaard, 2015, European Journal of Human Genetics.

Sycp 1 functions in synaptonemal complex assembly , meiotic recombination and XY body formation

Christa, A. Pastink, M. Ooms, 2007 .

Schizosaccharomyces pombe

Harry, P. V. Buul, J. Essers, 2007 .

SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))

M. Srebniak, D. Van Opstal, F. Vries, 2014, Prenatal diagnosis.

Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2

G. Driessen, L. Daxinger, S. M. van der Maarel, 2017, Clinical genetics.

Whole‐genome array as a first‐line cytogenetic test in prenatal diagnosis

M. Knapen, F. D. de Vries, R. Galjaard, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

An analysis of replication errors made by a defective T4 DNA polymerase

F. Vries, A. Waard, Ch. J. H. Swart-Idenburg, 2004, Molecular and General Genetics MGG.

Prenatal and postnatal findings in small‐for‐gestational‐age fetuses without structural ultrasound anomalies at 18–24 weeks

D. Papatsonis, M. Knapen, F. D. de Vries, 2017, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs

M. Knapen, J. Knijnenburg, R. Galjaard, 2015, European Journal of Human Genetics.