de Die-Smulders CE - Search Results

1

[Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].

de Die-Smulders CE, Land JA, Dreesen JC, Coonen E, Evers JL, Geraedts JP. de Die-Smulders CE, et al. Ned Tijdschr Geneeskd. 2004 Dec 11;148(50):2491-6. Ned Tijdschr Geneeskd. 2004. PMID: 15638197 Dutch.

2

Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family.

de Die-Smulders CE, Höweler CJ, Mirandolle JF, Brunner HG, Hovers V, Brüggenwirth H, Smeets HJ, Geraedts JP. de Die-Smulders CE, et al. J Med Genet. 1994 Aug;31(8):595-601. doi: 10.1136/jmg.31.8.595. J Med Genet. 1994. PMID: 7815415 Free PMC article.

3

The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes.

Zwamborn-Hanssen AM, Bijlsma JB, Hennekam EF, Lindhout D, Beemer FA, Bakker E, Kleijer WJ, de France HF, de Die-Smulders CE, Duran M, van Gennip AH, van Mens JT, Pearson PL, Mantel G, Verhage RE, Geraedts JP. Zwamborn-Hanssen AM, et al. Am J Med Genet. 1997 Jun 27;70(4):444-7. doi: 10.1002/(sici)1096-8628(19970627)70:4<444::aid-ajmg20>3.0.co;2-g. Am J Med Genet. 1997. PMID: 9182789

4

Paternal transmission of congenital myotonic dystrophy.

de Die-Smulders CE, Smeets HJ, Loots W, Anten HB, Mirandolle JF, Geraedts JP, Höweler CJ. de Die-Smulders CE, et al. J Med Genet. 1997 Nov;34(11):930-3. doi: 10.1136/jmg.34.11.930. J Med Genet. 1997. PMID: 9391889 Free PMC article.

5

Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH.

Martini E, von Bergh AR, Coonen E, de Die-Smulders CE, Hopman AH, Ramaekers FC, Geraedts JP. Martini E, et al. Hum Genet. 1998 Feb;102(2):157-65. doi: 10.1007/s004390050670. Hum Genet. 1998. PMID: 9521583

6

Age and causes of death in adult-onset myotonic dystrophy.

de Die-Smulders CE, Höweler CJ, Thijs C, Mirandolle JF, Anten HB, Smeets HJ, Chandler KE, Geraedts JP. de Die-Smulders CE, et al. Brain. 1998 Aug;121 ( Pt 8):1557-63. doi: 10.1093/brain/121.8.1557. Brain. 1998. PMID: 9712016

7

Preimplantation genetic diagnosis of spinal muscular atrophy.

Dreesen JC, Bras M, de Die-Smulders C, Dumoulin JC, Cobben JM, Evers JL, Smeets HJ, Geraedts JP. Dreesen JC, et al. Mol Hum Reprod. 1998 Sep;4(9):881-5. doi: 10.1093/molehr/4.9.881. Mol Hum Reprod. 1998. PMID: 9783849

8

[Genetic diagnosis of IVF embryos: preliminary results from 'preimplantation genetic diagnoses' in the Netherlands].

de Die-Smulders CE, Geraedts JP, Dreesen JC, Coonen E, Land JA. de Die-Smulders CE, et al. Ned Tijdschr Geneeskd. 1998 Nov 7;142(45):2441-4. Ned Tijdschr Geneeskd. 1998. PMID: 10028321 Dutch.

9

Preimplantation genetic diagnosis of a reciprocal translocation t(3;11)(q27.3;q24.3) in siblings.

Coonen E, Martini E, Dumoulin JC, Hollanders-Crombach HT, de Die-Smulders C, Geraedts JP, Hopman AH, Evers JL. Coonen E, et al. Mol Hum Reprod. 2000 Mar;6(3):199-206. doi: 10.1093/molehr/6.3.199. Mol Hum Reprod. 2000. PMID: 10694265

10

Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)(n) repeat detection.

Drüsedau M, Dreesen JC, De Die-Smulders C, Hardy K, Bras M, Dumoulin JC, Evers JL, Smeets HJ, Geraedts JP, Herbergs J. Drüsedau M, et al. Mol Hum Reprod. 2004 Jan;10(1):71-5. doi: 10.1093/molehr/gah008. Mol Hum Reprod. 2004. PMID: 14665709

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