Wijmenga C - Search Results

1

Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite.

Giltay JC, Brunt T, Beemer FA, Wit JM, van Amstel HK, Pearson PL, Wijmenga C. Giltay JC, et al. Among authors: wijmenga c. Am J Hum Genet. 1998 Apr;62(4):937-40. doi: 10.1086/301796. Am J Hum Genet. 1998. PMID: 9529354 Free PMC article.

2

Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.

Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Wijmenga C, et al. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.

3

Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease.

Wijmenga C, Müller T, Murli IS, Brunt T, Feichtinger H, Schönitzer D, Houwen RH, Müller W, Sandkuijl LA, Pearson PL. Wijmenga C, et al. Eur J Hum Genet. 1998 Nov-Dec;6(6):624-8. doi: 10.1038/sj.ejhg.5200235. Eur J Hum Genet. 1998. PMID: 9887382

4

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q.

Scheres JM, de Pater JM, Stoutenbeek P, Wijmenga C, Rosenberg C, Pearson PL. Scheres JM, et al. Among authors: wijmenga c. Cancer Genet Cytogenet. 1999 Nov;115(1):1-10. doi: 10.1016/s0165-4608(99)00049-7. Cancer Genet Cytogenet. 1999. PMID: 10565292

5

Defining the genetic contribution of type 2 diabetes mellitus.

van Tilburg J, van Haeften TW, Pearson P, Wijmenga C. van Tilburg J, et al. Among authors: wijmenga c. J Med Genet. 2001 Sep;38(9):569-78. doi: 10.1136/jmg.38.9.569. J Med Genet. 2001. PMID: 11546824 Free PMC article. Review.

6

Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.

van de Sluis BJ, Breen M, Nanji M, van Wolferen M, de Jong P, Binns MM, Pearson PL, Kuipers J, Rothuizen J, Cox DW, Wijmenga C, van Oost BA. van de Sluis BJ, et al. Among authors: wijmenga c. Hum Mol Genet. 1999 Mar;8(3):501-7. doi: 10.1093/hmg/8.3.501. Hum Mol Genet. 1999. PMID: 9949209

7

Genetic variation in ICF syndrome: evidence for genetic heterogeneity.

Wijmenga C, Hansen RS, Gimelli G, Björck EJ, Davies EG, Valentine D, Belohradsky BH, van Dongen JJ, Smeets DF, van den Heuvel LP, Luyten JA, Strengman E, Weemaes C, Pearson PL. Wijmenga C, et al. Hum Mutat. 2000 Dec;16(6):509-17. doi: 10.1002/1098-1004(200012)16:6<509::AID-HUMU8>3.0.CO;2-V. Hum Mutat. 2000. PMID: 11102980 Review.

8

The tissue transglutaminase gene is not a primary factor predisposing to celiac disease.

van Belzen MJ, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: wijmenga c. Am J Gastroenterol. 2001 Dec;96(12):3337-40. doi: 10.1111/j.1572-0241.2001.05335.x. Am J Gastroenterol. 2001. PMID: 11774946

9

Anticipation in familial intracranial aneurysms in consecutive generations.

Struycken PM, Pals G, Limburg M, Pronk JC, Wijmenga C, Pearson PL, Luijten JA, van den Berg JS, Vermeulen M, Rinkel GJ, Westerveld A. Struycken PM, et al. Among authors: wijmenga c. Eur J Hum Genet. 2003 Oct;11(10):737-43. doi: 10.1038/sj.ejhg.5201039. Eur J Hum Genet. 2003. PMID: 14512962

10

Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population.

van Tilburg JH, Sandkuijl LA, Franke L, Strengman E, Pearson PL, van Haeften TW, Wijmenga C. van Tilburg JH, et al. Among authors: wijmenga c. Eur J Clin Invest. 2003 Dec;33(12):1070-4. doi: 10.1111/j.1365-2362.2003.01276.x. Eur J Clin Invest. 2003. PMID: 14636289

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