Smeets D - Search Results

1

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. Among authors: smeets d. Am J Med Genet. 1994 Jul 15;51(4):497-500. doi: 10.1002/ajmg.1320510440. Am J Med Genet. 1994. PMID: 7943027

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. Among authors: smeets d. 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. Among authors: smeets d. 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

Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.

van Oost BA, Smits A, Dreesen JC, Smeets D, Perdon L, van Bennekom CA, Dahl N, Bakker E, Oostra BA. van Oost BA, et al. Among authors: smeets d. Am J Med Genet. 1991 Feb-Mar;38(2-3):328-31. doi: 10.1002/ajmg.1320380232. Am J Med Genet. 1991. PMID: 2018075

5

Penetrance estimate of the fra(X) gene using Pointer versus direct estimate.

de Haan AF, Smits AP, Smeets DF, van Oost BA. de Haan AF, et al. Among authors: smeets df. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):361-4. doi: 10.1002/ajmg.1320430156. Am J Med Genet. 1992. PMID: 1605213

6

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: smeets df. 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

7

Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.

Hamel BC, Smits AP, de Graaff E, Smeets DF, Schoute F, Eussen BH, Knight SJ, Davies KE, Assman-Hulsmans CF, Oostra BA. Hamel BC, et al. Among authors: smeets df. Am J Hum Genet. 1994 Nov;55(5):923-31. Am J Hum Genet. 1994. PMID: 7977354 Free PMC article.

8

The fragile X syndrome: no evidence for any recent mutations.

Smits AP, Dreesen JC, Post JG, Smeets DF, de Die-Smulders C, Spaans-van der Bijl T, Govaerts LC, Warren ST, Oostra BA, van Oost BA. Smits AP, et al. Among authors: smeets df. J Med Genet. 1993 Feb;30(2):94-6. doi: 10.1136/jmg.30.2.94. J Med Genet. 1993. PMID: 8445628 Free PMC article.

9

Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.

Yntema HG, Hamel BC, Smits AP, van Roosmalen T, van den Helm B, Kremer H, Ropers HH, Smeets DF, van Bokhoven H. Yntema HG, et al. Among authors: smeets df. J Med Genet. 1998 Oct;35(10):801-5. doi: 10.1136/jmg.35.10.801. J Med Genet. 1998. PMID: 9783701 Free PMC article.

10

Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.

Hamel BC, Smits AP, van den Helm B, Smeets DF, Knoers NV, van Roosmalen T, Thoonen GH, Assman-Hulsmans CF, Ropers HH, Mariman EC, Kremer H. Hamel BC, et al. Among authors: smeets df. Am J Med Genet. 1999 Jul 30;85(3):290-304. Am J Med Genet. 1999. PMID: 10398246

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