Victor H. Garritsen

Molecular analysis of mutations in DNA polymerase η in xeroderma pigmentosum-variant patients

Bernard C. Broughton, Agnès Cordonnier, Wim J. Kleijer et al. · Proceedings of the National Academy of Sciences · 2002 · 164 citations · Full text

Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy

John M. Graham, Kwame Anyane‐Yeboa, Anja Raams et al. · The American Journal of Human Genetics · 2001 · 133 citations · Full text

Triplet Pregnancy, Genetic Disorder, Genetics +7

Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families

Wim J. Kleijer, Victor H. Garritsen, Michael Linnebank et al. · Journal of Inherited Metabolic Disease · 2002 · 44 citations

Xeroderma Pigmentosum Group G with Severe Neurological Involvement and Features of Cockayne Syndrome in Infancy

Dimitrios Zafeiriou, Fabrizio Thorel, Alexander Andreou et al. · Pediatric Research · 2001 · 40 citations · Full text

Developmental Biology, Neuroanatomy, Pathology +5

Prenatal diagnosis of the Cockayne syndrome: survey of 15 years experience

Wim J. Kleijer, Marianne L. T. van der Sterre, Victor H. Garritsen et al. · Prenatal Diagnosis · 2006 · 28 citations · Full text