T.J.R. van de Pol

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

Frans P.M. Cremers, R. A. Pfeiffer, T.J.R. van de Pol et al. · Human Genetics · 1987 · 79 citations

Chromatin, Cytogenetics, X Chromosome +10

Complete Exon–Intron Structure of the Retina-Specific ATP Binding Transporter Gene (ABCR) Allows the Identification of Novel Mutations Underlying Stargardt Disease

S. Gerber, Jean‐Michel Rozet, T.J.R. van de Pol et al. · Genomics · 1998 · 78 citations

Complete Exon–intron Structure, Natural Sciences, Molecular Biology +6

Deletion of the DXS165 locus in patients with classical Choroideremia

Frans P.M. Cremers, Frank Brunsmann, T.J.R. van de Pol et al. · Clinical Genetics · 1987 · 37 citations

Genetic fine mapping of the gene for recessive Stargardt disease

Carel B. Hoyng, Francis A.M. Poppelaars, T.J.R. van de Pol et al. · Human Genetics · 1996 · 31 citations

Mendelian Disorder, Genetic Disorder, Genetics +9

Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs☆

Mirjam W.J. Luijendijk, T.J.R. van de Pol, Gerard van Duijnhoven et al. · Genomics · 2003 · 23 citations

Genetics, Molecular Genetics, Auditory Science +16