van de Kamp JJ - Search Results

1

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

Bröcker-Vriends AH, Rosendaal FR, van Houwelingen JC, Bakker E, van Ommen GJ, van de Kamp JJ, Briët E. Bröcker-Vriends AH, et al. Among authors: van de kamp jj, van ommen gj, van houwelingen jc. J Med Genet. 1991 Oct;28(10):672-80. doi: 10.1136/jmg.28.10.672. J Med Genet. 1991. PMID: 1682494 Free PMC article.

2

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

3

First trimester prenatal diagnosis of haemophilia A: two years' experience.

Bröcker-Vriends AH, Briët E, Kanhai HH, Bakker E, Dreesen JC, Leschot NJ, Van de Kamp JJ, Pearson PL. Bröcker-Vriends AH, et al. Among authors: van de kamp jj. Prenat Diagn. 1988 Jul;8(6):411-21. doi: 10.1002/pd.1970080605. Prenat Diagn. 1988. PMID: 2905454

4

The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.

Bröcker-Vriends AH, Bakker E, Kanhai HH, van Ommen GJ, Reitsma PH, van de Kamp JJ, Briët E. Bröcker-Vriends AH, et al. Among authors: van de kamp jj, van ommen gj. Ann Hematol. 1992 Jan;64(1):2-11. doi: 10.1007/BF01811464. Ann Hematol. 1992. PMID: 1739755 Review.

5

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

6

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

7

Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms.

Bröcker-Vriends AH, Briët E, Quadt R, Dreesen JC, Bakker E, Claassen-Tegelaar R, Kanhai HH, van de Kamp JJ, Pearson PL. Bröcker-Vriends AH, et al. Among authors: van de kamp jj. Thromb Haemost. 1987 Apr 7;57(2):131-6. Thromb Haemost. 1987. PMID: 2885943

8

Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism.

Bröcker-Vriends AH, Briët E, Quadt R, Bertina RM, van der Linden IK, van de Kamp JJ, Pearson PL, Veltkamp JJ. Bröcker-Vriends AH, et al. Among authors: van der linden ik, van de kamp jj. Thromb Haemost. 1985 Aug 30;54(2):506-9. Thromb Haemost. 1985. PMID: 3001965

9

Monosomy 8p: an easily overlooked syndrome.

Bröcker-Vriends AH, Mooij PD, van Bel F, Beverstock GC, van de Kamp JJ. Bröcker-Vriends AH, et al. Among authors: van de kamp jj, van bel f. J Med Genet. 1986 Apr;23(2):153-4. doi: 10.1136/jmg.23.2.153. J Med Genet. 1986. PMID: 3712390 Free PMC article.

10

[Search for the carrier state of hemophilia B using restriction fragment length polymorphism].

Briët E, Bröcker-Vriends A, Quadt R, Bertina RM, van der Linden IK, van de Kamp JJ, Pearson PL, Veltkamp JJ. Briët E, et al. Among authors: van der linden ik, van de kamp jj. Ned Tijdschr Geneeskd. 1985 Jun 15;129(24):1141-5. Ned Tijdschr Geneeskd. 1985. PMID: 2991783 Dutch. No abstract available.

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