van Oost BA - Search Results

1

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: van oost ba. Am J Hum Genet. 1993 Nov;53(5):1016-23. Am J Hum Genet. 1993. PMID: 8213829 Free PMC article.

2

Parental origin of the fra(X) gene is a major determinant of the cytogenetic expression and the CGG repeat length in female carriers.

Smits A, Smeets D, Dreesen J, Hamel B, de Haan A, van Oost B. Smits A, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):261-7. doi: 10.1002/ajmg.1320430141. Am J Med Genet. 1992. PMID: 1605199

3

High prevalence of the fra(X) syndrome cannot be explained by a high mutation rate.

Smits A, Smeets D, Hamel B, Dreesen J, van Oost B. Smits A, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):345-52. doi: 10.1002/ajmg.1320430153. Am J Med Genet. 1992. PMID: 1605209

4

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: van oost ba. 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.

5

Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male.

Smits AP, van Oost BA, de Haan AF, Hamel BC, Dreesen JC, Smeets DF. Smits AP, et al. Among authors: van oost ba. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):365-72. doi: 10.1002/ajmg.1320430157. Am J Med Genet. 1992. PMID: 1605214

6

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: van oost ba, van den biezenbos jb. Brain. 1991 Oct;114 ( Pt 5):2303-11. doi: 10.1093/brain/114.5.2303. Brain. 1991. PMID: 1933246

7

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: van oost ba. Hum Genet. 1989 Mar;81(4):308-10. doi: 10.1007/BF00283680. Hum Genet. 1989. PMID: 2703233

8

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: van oost ba. 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.

9

Prediction of mental status in carriers of the fragile X mutation using CGG repeat length.

Smits A, Smeets D, Hamel B, Dreesen J, de Haan A, van Oost B. Smits A, et al. Am J Med Genet. 1994 Jul 15;51(4):497-500. doi: 10.1002/ajmg.1320510440. Am J Med Genet. 1994. PMID: 7943027

10

Eye movement disorder: an early expression of the myotonic dystrophy gene?

ter Bruggen JP, Tijssen CC, Brunner HG, van Oost BA, Bastiaensen LA. ter Bruggen JP, et al. Among authors: van oost ba. Muscle Nerve. 1992 Mar;15(3):358-61. doi: 10.1002/mus.880150315. Muscle Nerve. 1992. PMID: 1557084

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