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Genomics|January 20, 1995
Localization of the human phosphatidylinositol-specific phospholipase c beta 3 gene (PLCB3) within chromosome band 11q13R J Sinke, A G Geurts van KesselNederlands Tijdschrift Voor Geneeskunde|April 16, 2004
[From gene to disease; autosomal dominant cerebellar ataxias]H P Kremer, B P van de Warrenburg, R J SinkeThe British Journal of Dermatology|April 7, 2011
Junctional epidermolysis bullosa of late onset explained by mutations in COL17A1W Y Yuen, H H Pas, R J Sinke, et al.Nederlands Tijdschrift Voor Geneeskunde|August 29, 2003
[Developmental disorder in girls due to Rett syndrome]D M Pruissen, R J Sinke, P A Terhal, et al.Genes, Chromosomes & Cancer|March 1, 1993
Uniparental origin of i(12p) in human germ cell tumorsR J Sinke, R F Suijkerbuijk, B de Jong, et al.The British Journal of Dermatology|August 2, 2011
Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the NetherlandsW Y Yuen, H H Lemmink, K K van Dijk-Bos, et al.Genomics|February 1, 1992
Generation of a panel of somatic cell hybrids containing fragments of human chromosome 12P by X-ray irradiation and cell fusionR J Sinke, R F Suijkerbuijk, J Herbergs, et al.Genes, Chromosomes & Cancer|January 1, 1995
Definition of a new entity of malignant extragonadal germ cell tumorsJ van Echten, B de Jong, R J Sinke, et al.European Urology|January 1, 1993
Molecular cytogenetics of human germ cell tumours: i(12p) and related chromosomal anomaliesA Geurts van Kessel, R F Suijkerbuijk, R J Sinke, et al.Journal of Neurology|April 4, 2001
Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxiaH J Schelhaas, P F Ippel, G Hageman, et al.Pageof 5