van de Kamp JJ - Search Results

1

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

van der Steenstraten IM, Tibben A, Roos RA, van de Kamp JJ, Niermeijer MF. van der Steenstraten IM, et al. Among authors: van de kamp jj. Am J Hum Genet. 1994 Oct;55(4):618-25. Am J Hum Genet. 1994. PMID: 7942839 Free PMC article. Clinical Trial.

2

Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention.

Tibben A, Duivenvoorden HJ, Vegter-van der Vlis M, Niermeijer MF, Frets PG, van de Kamp JJ, Roos RA, Rooijmans HG, Verhage F. Tibben A, et al. Among authors: van de kamp jj. Am J Med Genet. 1993 Oct 15;48(3):137-44. doi: 10.1002/ajmg.1320480305. Am J Med Genet. 1993. PMID: 8291567

3

Understanding the low uptake of presymptomatic DNA testing for Huntington's disease.

Tibben A, Niermeijer MF, Roos RA, Vegter van de Vlis M, Frets PG, van Ommen GJ, van de Kamp JJ, Verhage F. Tibben A, et al. Among authors: van de kamp jj, van ommen gj. Lancet. 1992 Dec 5;340(8832):1416. doi: 10.1016/0140-6736(92)92610-r. Lancet. 1992. PMID: 1360126 No abstract available.

4

[Presymptomatic DNA diagnosis in Huntington's chorea: reactions to the certainty of not being a genetic carrier].

Tibben A, Vegter-van der Vlis M, Roos RA, van de Kamp JJ, Frets PG, Verhage F. Tibben A, et al. Among authors: van de kamp jj. Ned Tijdschr Geneeskd. 1990 Apr 7;134(14):701-4. Ned Tijdschr Geneeskd. 1990. PMID: 2139181 Dutch.

5

Intermittent thrombocytopenia and absent radii: report of a patient with additional unusual manifestations.

van Haeringen A, Veenstra F, Maaswinkel-Mooij PD, van de Kamp JJ. van Haeringen A, et al. Among authors: van de kamp jj. Am J Med Genet. 1989 Oct;34(2):202-6. doi: 10.1002/ajmg.1320340214. Am J Med Genet. 1989. PMID: 2816998

6

Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program.

Tibben A, Frets PG, van de Kamp JJ, Niermeijer MF, Vegter-van der Vlis M, Roos RA, van Ommen GJ, Duivenvoorden HJ, Verhage F. Tibben A, et al. Among authors: van de kamp jj. Am J Med Genet. 1993 May 1;48(1):10-6. doi: 10.1002/ajmg.1320480105. Am J Med Genet. 1993. PMID: 8357031

7

Attitudes of Dutch general practitioners towards presymptomatic DNA-testing for Huntington disease.

Thomassen R, Tibben A, Niermeijer MF, van der Does E, van de Kamp JJ, Verhage F. Thomassen R, et al. Among authors: van de kamp jj, van der does e. Clin Genet. 1993 Feb;43(2):63-8. doi: 10.1111/j.1399-0004.1993.tb04428.x. Clin Genet. 1993. PMID: 8448902

8

On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program.

Tibben A, Frets PG, van de Kamp JJ, Niermeijer MF, Vegtervan der Vlis M, Roos RA, Rooymans HG, van Ommen GJ, Verhage F. Tibben A, et al. Among authors: van de kamp jj. Am J Med Genet. 1993 Jul 15;48(2):103-11. doi: 10.1002/ajmg.1320480209. Am J Med Genet. 1993. PMID: 8362926

9

The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986.

Veenema H, Beverstock GC, de Koning T, Pearson PL, van de Kamp JJ. Veenema H, et al. Among authors: van de kamp jj, de koning t. Clin Genet. 1988 Jun;33(6):410-7. doi: 10.1111/j.1399-0004.1988.tb03473.x. Clin Genet. 1988. PMID: 3168313

10

Somatic origin of inherited haemophilia A.

Bröcker-Vriends AH, Briët E, Dreesen JC, Bakker B, Reitsma P, Pannekoek H, van de Kamp JJ, Pearson PL. Bröcker-Vriends AH, et al. Among authors: van de kamp jj. Hum Genet. 1990 Aug;85(3):288-92. doi: 10.1007/BF00206748. Hum Genet. 1990. PMID: 1975557

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