Wieringa B - Search Results

1

Brief report: reverse mutation in myotonic dystrophy.

Brunner HG, Jansen G, Nillesen W, Nelen MR, de Die CE, Höweler CJ, van Oost BA, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. Among authors: wieringa b. N Engl J Med. 1993 Feb 18;328(7):476-80. doi: 10.1056/NEJM199302183280705. N Engl J Med. 1993. PMID: 8421477 Free article. No abstract available.

2

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Brunner HG, Brüggenwirth HT, Nillesen W, Jansen G, Hamel BC, Hoppe RL, de Die CE, Höweler CJ, van Oost BA, Wieringa B, et al. Brunner HG, et al. Among authors: wieringa b. Am J Hum Genet. 1993 Nov;53(5):1016-23. Am J Hum Genet. 1993. PMID: 8213829 Free PMC article.

3

[An unstable mutation as cause of myotonic dystrophy].

Brunner HG, Höweler CJ, Smeets HJ, Wieringa B. Brunner HG, et al. Among authors: wieringa b. Ned Tijdschr Geneeskd. 1993 Nov 27;137(48):2468-72. Ned Tijdschr Geneeskd. 1993. PMID: 8272119 Review. Dutch. No abstract available.

4

Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) gene.

Jansen G, Coerwinkel-Driessen M, Nillesen W, Brunner H, Wieringa B. Jansen G, et al. Among authors: wieringa b. Hum Mol Genet. 1993 Mar;2(3):333. doi: 10.1093/hmg/2.3.333. Hum Mol Genet. 1993. PMID: 8499928 No abstract available.

5

Presymptomatic diagnosis of myotonic dystrophy.

Brunner HG, Nillesen W, van Oost BA, Jansen G, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. Among authors: wieringa b. J Med Genet. 1992 Nov;29(11):780-4. doi: 10.1136/jmg.29.11.780. J Med Genet. 1992. PMID: 1453426 Free PMC article.

6

Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locus.

Smeets HJ, Hermens R, Brunner HG, Ropers HH, Wieringa B. Smeets HJ, et al. Among authors: wieringa b. Genomics. 1991 Feb;9(2):257-63. doi: 10.1016/0888-7543(91)90250-i. Genomics. 1991. PMID: 1840564

7

Myotonic dystrophy. Predictive value of normal results on clinical examination.

Brunner HG, Smeets HJ, Nillesen W, van Oost BA, van den Biezenbos JB, Joosten EM, Pinckers AJ, Hamel BC, Theeuwes AG, Wieringa B, et al. Brunner HG, et al. Among authors: wieringa b. Brain. 1991 Oct;114 ( Pt 5):2303-11. doi: 10.1093/brain/114.5.2303. Brain. 1991. PMID: 1933246

8

Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy.

Brunner HG, Spaans F, Smeets HJ, Coerwinkel-Driessen M, Hulsebos T, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: wieringa b. Neurology. 1991 Jan;41(1):80-4. doi: 10.1212/wnl.41.1.80. Neurology. 1991. PMID: 1985299

9

Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Smeets HJ, Brunner HG, Ropers HH, Wieringa B. Smeets HJ, et al. Among authors: wieringa b. Hum Genet. 1989 Oct;83(3):245-51. doi: 10.1007/BF00285165. Hum Genet. 1989. PMID: 2571562

10

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.

Brunner HG, Smeets H, Lambermon HM, Coerwinkel-Driessen M, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: wieringa b. Genomics. 1989 Oct;5(3):589-95. doi: 10.1016/0888-7543(89)90027-x. Genomics. 1989. PMID: 2575588

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