van Ommen GJ - Search Results

1

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.

Wijmenga C, Sandkuijl LA, Moerer P, van der Boorn N, Bodrug SE, Ray PN, Brouwer OF, Murray JC, van Ommen GJ, Padberg GW, et al. Wijmenga C, et al. Among authors: van der boorn n, van ommen gj. Am J Hum Genet. 1992 Aug;51(2):411-5. Am J Hum Genet. 1992. PMID: 1642239 Free PMC article.

2

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

Wijmenga C, van Deutekom JC, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: van ommen gj, van deutekom jc. Genomics. 1994 Jan 1;19(1):21-6. doi: 10.1006/geno.1994.1006. Genomics. 1994. PMID: 7910579

3

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit.

van Deutekom JC, Wijmenga C, van Tienhoven EA, Gruter AM, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. van Deutekom JC, et al. Among authors: van tienhoven ea, van ommen gj. Hum Mol Genet. 1993 Dec;2(12):2037-42. doi: 10.1093/hmg/2.12.2037. Hum Mol Genet. 1993. PMID: 8111371

4

Molecular genetics of facioscapulohumeral muscular dystrophy.

Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ. Wijmenga C, et al. Among authors: van ommen gj, van geel m, van deutekom jc. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):487-91. doi: 10.1016/0960-8966(93)90102-p. Neuromuscul Disord. 1993. PMID: 8186699 Review.

5

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region.

Wijmenga C, Wright TJ, Baan MJ, Padberg GW, Williamson R, van Ommen GJ, Hewitt JE, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: van ommen gj. Hum Mol Genet. 1993 Oct;2(10):1667-72. doi: 10.1093/hmg/2.10.1667. Hum Mol Genet. 1993. PMID: 8268920

6

Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity.

Oosterwijk JC, Richard G, van der Wielen MJ, van de Vosse E, Harth W, Sandkuijl LA, Bakker E, van Ommen GJ. Oosterwijk JC, et al. Among authors: van der wielen mj, van ommen gj, van de vosse e. Hum Genet. 1997 Oct;100(5-6):520-4. doi: 10.1007/s004390050546. Hum Genet. 1997. PMID: 9341865

7

De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.

van der Maarel SM, Deidda G, Lemmers RJ, van Overveld PG, van der Wielen M, Hewitt JE, Sandkuijl L, Bakker B, van Ommen GJ, Padberg GW, Frants RR. van der Maarel SM, et al. Among authors: van overveld pg, van der wielen m, van ommen gj. Am J Hum Genet. 2000 Jan;66(1):26-35. doi: 10.1086/302730. Am J Hum Genet. 2000. PMID: 10631134 Free PMC article.

8

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: van der mey ag, van gils ap, van ommen gj, van vliet m. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

9

Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population.

Skraastad MI, Van de Vosse E, Belfroid R, Höld K, Vegter-van der Vlis M, Sandkuijl LA, Bakker E, van Ommen GJ. Skraastad MI, et al. Among authors: van ommen gj, van de vosse e. Am J Hum Genet. 1992 Oct;51(4):730-5. Am J Hum Genet. 1992. PMID: 1415218 Free PMC article.

10

Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families.

Bergen AA, Van den Born LI, Schuurman EJ, Pinckers AJ, Van Ommen GJ, Bleekers-Wagemakers EM, Sandkuijl LA. Bergen AA, et al. Among authors: van den born li, van ommen gj. Ophthalmic Genet. 1995 Jun;16(2):63-70. doi: 10.3109/13816819509056914. Ophthalmic Genet. 1995. PMID: 7493158

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