OF Brouwer

A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum

J. van Reeuwijk, T. Roscioli, H. van Bokhoven, 2010, Clinical genetics.

Burst suppression on amplitude‐integrated electroencephalogram may be induced by midazolam: a report on three cases

OF Brouwer, H. Horst, A. Bos, 2004, Acta paediatrica.

Refinement of the chromosome 16 locus for benign familial infantile convulsions

J. Oosterwijk, G. Hageman, R R Frants, 2005, Clinical genetics.

A novel mutation in MED12 causes FG syndrome (Opitz–Kaveggia syndrome)

P. Rump, O. Brouwer, R. Hordijk, 2011, Clinical genetics.

A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum

J. van Reeuwijk, T. Roscioli, H. van Bokhoven, 2010, Clinical genetics.