Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Van de Kamp JJ"'
Autor:
R M Bertina, van der Linden Ik, Pearson Pl, Bröcker-Vriends Ah, Quadt R, Jan J. Veltkamp, Ernest Briët, van de Kamp Jj
Publikováno v:
Thrombosis and Haemostasis. 54:506-509
SummaryWe analysed DNA from individuals of five families with haemophilia B, including nineteen potential carriers. A genespecific probe was used to reveal a TaqI restriction-fragment length polymorphism. Segregation analysis of the polymorphic marke
Autor:
Claassen-Tegelaar R, van de Kamp Jj, Egbert Bakker, Ernest Briët, J. C. F. M. Dreesen, Kanhai Hh, Quadt R, Pearson Pl, A H J T Bröcker-Vriends
Publikováno v:
Thrombosis and Haemostasis. 57:131-136
SummaryWe performed DNA analysis in 20 families with haemophilia A in order to evaluate its usefulness for carrier detection and prenatal diagnosis.The polymorphic Bell site within intron 18 of the factor VIII gene and the extragenic TaqI and Bglll p
Autor:
Tibben A (AUTHOR), Niermeijer MF (AUTHOR), Roos RA (AUTHOR), Vegter van de Vlis M (AUTHOR), Frets PG (AUTHOR), van Ommen GJ (AUTHOR), van de Kamp JJ (AUTHOR), Verhage F (AUTHOR), Tibben, A (AUTHOR), Niermeijer, M F (AUTHOR), Roos, R A (AUTHOR), Vegter van de Vlis, M (AUTHOR), Frets, P G (AUTHOR), van Ommen, G J (AUTHOR), van de Kamp, J J (AUTHOR), Verhage, F (AUTHOR)
Publikováno v:
Lancet. 12/5/1992, Vol. 340 Issue 8832, p1416-1416. 1p.
Autor:
Beverstock GC; Clinical Genetic Center, Leiden University Medical Center (LUMC), Leiden, The Netherlands., Bezrookove V, Mollevanger P, van de Kamp JJ, Pearson P, Kouwenberg JM, Rosenberg C
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2003 Oct 01; Vol. 122A (2), pp. 168-73.
Autor:
Weber B; Department of Chemical Pathology, Women's and Children's Hospital, North Adelaide, Australia., Guo XH, Kleijer WJ, van de Kamp JJ, Poorthuis BJ, Hopwood JJ
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 1999 Jan; Vol. 7 (1), pp. 34-44.
Autor:
Weber B; Lysosomal Diseases Research Unit, Department of Chemical Pathology, Women's & Children's Hospital, North Adelaide, Australia., van de Kamp JJ, Kleijer WJ, Guo XH, Blanch L, van Diggelen OP, Wevers R, Poorthuis BJ, Hopwood JJ
Publikováno v:
Journal of inherited metabolic disease [J Inherit Metab Dis] 1998 Jun; Vol. 21 (4), pp. 416-22.
Autor:
Landsmeer-Beker EA; Department of Paediatrics, University Hospital Leiden, The Netherlands., Massa GG, Maaswinkel-Mooy PD, van de Kamp JJ, Papapoulos SE
Publikováno v:
European journal of pediatrics [Eur J Pediatr] 1997 Oct; Vol. 156 (10), pp. 792-4.
Autor:
Oosterwijk JC; Department of Clinical Genetics, Leiden University Hospital, The Netherlands. J.C.Oosterwijk@MED.RUG.NL, Mesker WE, Ouwerkerk MC, Knepflé CF, van der Burg MJ, Wiesmeijer CC, Beverstock GC, Losekoot M, Bernini LF, van Ommen GJ, van de Kamp JJ, Kanhai HH, Tanke HJ
Publikováno v:
Early human development [Early Hum Dev] 1996 Dec 30; Vol. 47 Suppl, pp. S95-7.
Autor:
van der Steenstraten IM; Department of Medical Psychology and Psychotherapy, Erasmus University, Rotterdam, The Netherlands., Tibben A, Roos RA, van de Kamp JJ, Niermeijer MF
Publikováno v:
American journal of human genetics [Am J Hum Genet] 1994 Oct; Vol. 55 (4), pp. 618-25.
Autor:
Tibben A; Department of Medical Psychology and Psychotherapy, Erasmus University Rotterdam, The Netherlands., Duivenvoorden HJ, Vegter-van der Vlis M, Niermeijer MF, Frets PG, van de Kamp JJ, Roos RA, Rooijmans HG, Verhage F
Publikováno v:
American journal of medical genetics [Am J Med Genet] 1993 Oct 15; Vol. 48 (3), pp. 137-44.