G.J.B. van Ommen

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Alan H. Beggs, Mary B. Moyer, S. Scherpf et al. · PubMed · 1989 · 961 citations

Medicine, Genetics, Molecular Genetics +10

PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

Egbert Bakker, Nicole Goor, Klaus Wrogemann et al. · The Lancet · 1985 · 376 citations

Medicine, Genetics, Molecular Genetics +7

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A

Linda J. Valentijn, Pieter A. Bolhuis, Ina Zorn et al. · Nature Genetics · 1992 · 320 citations

Medicine, Molecular Genetics, Neurology +14

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

Dorien J.M. Peters, Lia Spruit, Jasper J. Saris et al. · Nature Genetics · 1993 · 272 citations

Life Sciences, Genetics, Molecular Genetics +12

Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers

Claudia Ruivenkamp, Tom van Wezel, Carlo Zanon et al. · Nature Genetics · 2002 · 261 citations

Medicine, Genetics, Molecular Genetics +10