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Stroke|August 7, 2004
Association of polymorphisms and haplotypes in the elastin gene in Dutch patients with sporadic aneurysmal subarachnoid hemorrhageY M Ruigrok, U Seitz, S Wolterink, et al.
Genes and Immunity|May 6, 2005
Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch populationA Zhernakova, P Eerligh, C Wijmenga, et al.
Human Molecular Genetics|October 1, 1993
Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11T J Wright, C Wijmenga, L N Clark, et al.
Cancer Genetics and Cytogenetics|November 24, 1999
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.
Muscle & Nerve. Supplement|January 1, 1995
Facioscapulohumeral muscular dystrophy in the Dutch populationG W Padberg, R R Frants, O F Brouwer, et al.
Lancet (London, England)|September 15, 1990
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4C Wijmenga, R R Frants, O F Brouwer, et al.
Muscle & Nerve. Supplement|April 12, 2013
Facioscapulohumeral muscular dystrophy in the Dutch populationG W Padberg, R R Frants, O F Brouwer, et al.
Genomics|April 10, 1995
Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pterC Wijmenga, N A Speck, N C Dracopoli, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 1996
Core binding factor beta-smooth muscle myosin heavy chain chimeric protein involved in acute myeloid leukemia forms unusual nuclear rod-like structures in transformed NIH 3T3 cellsC Wijmenga, P E Gregory, A Hajra, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1999
The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndromeR S Hansen, C Wijmenga, P Luo, et al.
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