Victor H. Garritsen

Statistics

Publications

Citations

521

H-Index

Active since

2000

Affiliations

Erasmus University Rotterdam(Current)

Erasmus MC

University Hospital Münster

State Research Institute of Organic Chemistry and Technology

Victor H. Garritsen is an author at Erasmus University Rotterdam specializing in prenatal diagnosis, prenatal molecular diagnosis, and genetic disorders.

Publications per year

2000–2007

Publications

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 · 165 citations

Life Sciences, Genetics, Molecular Biology +17

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 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

Life Sciences, Genetics, Molecular Genetics +8

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

Medicine, Neurology, Pediatrics +14

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

Medicine, Molecular Biology, Obstetrics +13

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