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Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22.
Prenat Diagn. 1997 Jan;17(1):81-6. doi: 10.1002/(sici)1097-0223(199701)17:1<81::aid-pd29>3.0.co;2-v.
Prenat Diagn. 1997.
PMID: 9021833
An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.
Redeker E, Hoovers JM, Alders M, van Moorsel CJ, Ivens AC, Gregory S, Kalikin L, Bliek J, de Galan L, van den Bogaard R, et al.
Redeker E, et al. Among authors: van den bogaard r.
Genomics. 1994 Jun;21(3):538-50. doi: 10.1006/geno.1994.1312.
Genomics. 1994.
PMID: 7959730
Free article.
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Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families.
Fijen CA, van den Bogaard R, Daha MR, Dankert J, Mannens M, Kuijper EJ.
Fijen CA, et al. Among authors: van den bogaard r.
Eur J Clin Invest. 1996 Oct;26(10):902-6. doi: 10.1111/j.1365-2362.1996.tb02136.x.
Eur J Clin Invest. 1996.
PMID: 8911864
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Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
van den Bogaard R, Fijen CA, Schipper MG, de Galan L, Kuijper EJ, Mannens MM.
van den Bogaard R, et al.
Eur J Hum Genet. 2000 Jul;8(7):513-8. doi: 10.1038/sj.ejhg.5200496.
Eur J Hum Genet. 2000.
PMID: 10909851
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Properdin deficiency: molecular basis and disease association.
Fijen CA, van den Bogaard R, Schipper M, Mannens M, Schlesinger M, Nordin FG, Dankert J, Daha MR, Sjöholm AG, Truedsson L, Kuijper EJ.
Fijen CA, et al. Among authors: van den bogaard r.
Mol Immunol. 1999 Sep-Oct;36(13-14):863-7. doi: 10.1016/s0161-5890(99)00107-8.
Mol Immunol. 1999.
PMID: 10698340
Review.
No abstract available.
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Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.
van Den Bosch BJ, de Coo RF, Scholte HR, Nijland JG, van Den Bogaard R, de Visser M, de Die-Smulders CE, Smeets HJ.
van Den Bosch BJ, et al. Among authors: van den bogaard r.
Nucleic Acids Res. 2000 Oct 15;28(20):E89. doi: 10.1093/nar/28.20.e89.
Nucleic Acids Res. 2000.
PMID: 11024191
Free PMC article.
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A novel polymorphic GATA site in the human IL-12Rbeta2 promoter region affects transcriptional activity.
van Rietschoten JG, Westland R, van den Bogaard R, Nieste-Otter MA, van Veen A, Jonkers RE, van der Pouw Kraan TC, den Hartog MT, Wierenga EA.
van Rietschoten JG, et al. Among authors: van den bogaard r.
Tissue Antigens. 2004 Jun;63(6):538-46. doi: 10.1111/j.0001-2815.2004.00223.x.
Tissue Antigens. 2004.
PMID: 15140029
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ACE I/D polymorphism is associated with mortality in a cohort study of patients starting with dialysis.
van der Sman-de Beer F, Verhagen C, Rombach SM, Boorsma P, van Manen JG, Korevaar JC, van den Bogaard R, Boeschoten EW, Krediet RT, Navis GJ, Vandenbroucke JP, Dekker FW; NECOSAD Study Group.
van der Sman-de Beer F, et al. Among authors: van den bogaard r.
Kidney Int. 2005 Nov;68(5):2237-43. doi: 10.1111/j.1523-1755.2005.00681.x.
Kidney Int. 2005.
PMID: 16221224
Free article.
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