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BRCA Testing by Single-Molecule Molecular Inversion Probes.
Clin Chem. 2017 Feb;63(2):503-512. doi: 10.1373/clinchem.2016.263897. Epub 2016 Dec 14.
Clin Chem. 2017.
PMID: 27974384
Translating sanger-based routine DNA diagnostics into generic massive parallel ion semiconductor sequencing.
Diekstra A, Bosgoed E, Rikken A, van Lier B, Kamsteeg EJ, Tychon M, Derks RC, van Soest RA, Mensenkamp AR, Scheffer H, Neveling K, Nelen MR.
Diekstra A, et al. Among authors: van lier b.
Clin Chem. 2015 Jan;61(1):154-62. doi: 10.1373/clinchem.2014.225250. Epub 2014 Oct 1.
Clin Chem. 2015.
PMID: 25274553
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A de novo paradigm for mental retardation.
Vissers LE, de Ligt J, Gilissen C, Janssen I, Steehouwer M, de Vries P, van Lier B, Arts P, Wieskamp N, del Rosario M, van Bon BW, Hoischen A, de Vries BB, Brunner HG, Veltman JA.
Vissers LE, et al. Among authors: van lier b.
Nat Genet. 2010 Dec;42(12):1109-12. doi: 10.1038/ng.712. Epub 2010 Nov 14.
Nat Genet. 2010.
PMID: 21076407
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Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.
Gilissen C, Arts HH, Hoischen A, Spruijt L, Mans DA, Arts P, van Lier B, Steehouwer M, van Reeuwijk J, Kant SG, Roepman R, Knoers NV, Veltman JA, Brunner HG.
Gilissen C, et al. Among authors: van lier b.
Am J Hum Genet. 2010 Sep 10;87(3):418-23. doi: 10.1016/j.ajhg.2010.08.004.
Am J Hum Genet. 2010.
PMID: 20817137
Free PMC article.
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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.
Hoischen A, van Bon BW, Gilissen C, Arts P, van Lier B, Steehouwer M, de Vries P, de Reuver R, Wieskamp N, Mortier G, Devriendt K, Amorim MZ, Revencu N, Kidd A, Barbosa M, Turner A, Smith J, Oley C, Henderson A, Hayes IM, Thompson EM, Brunner HG, de Vries BB, Veltman JA.
Hoischen A, et al. Among authors: van lier b.
Nat Genet. 2010 Jun;42(6):483-5. doi: 10.1038/ng.581. Epub 2010 May 2.
Nat Genet. 2010.
PMID: 20436468
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De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.
Hoischen A, van Bon BW, Rodríguez-Santiago B, Gilissen C, Vissers LE, de Vries P, Janssen I, van Lier B, Hastings R, Smithson SF, Newbury-Ecob R, Kjaergaard S, Goodship J, McGowan R, Bartholdi D, Rauch A, Peippo M, Cobben JM, Wieczorek D, Gillessen-Kaesbach G, Veltman JA, Brunner HG, de Vries BB.
Hoischen A, et al. Among authors: van lier b.
Nat Genet. 2011 Jun 26;43(8):729-31. doi: 10.1038/ng.868.
Nat Genet. 2011.
PMID: 21706002
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MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study.
Makrythanasis P, van Bon BW, Steehouwer M, Rodríguez-Santiago B, Simpson M, Dias P, Anderlid BM, Arts P, Bhat M, Augello B, Biamino E, Bongers EM, Del Campo M, Cordeiro I, Cueto-González AM, Cuscó I, Deshpande C, Frysira E, Izatt L, Flores R, Galán E, Gener B, Gilissen C, Granneman SM, Hoyer J, Yntema HG, Kets CM, Koolen DA, Marcelis Cl, Medeira A, Micale L, Mohammed S, de Munnik SA, Nordgren A, Psoni S, Reardon W, Revencu N, Roscioli T, Ruiterkamp-Versteeg M, Santos HG, Schoumans J, Schuurs-Hoeijmakers JH, Silengo MC, Toledo L, Vendrell T, van der Burgt I, van Lier B, Zweier C, Reymond A, Trembath RC, Perez-Jurado L, Dupont J, de Vries BB, Brunner HG, Veltman JA, Merla G, Antonarakis SE, Hoischen A.
Makrythanasis P, et al. Among authors: van lier b.
Clin Genet. 2013 Dec;84(6):539-45. doi: 10.1111/cge.12081. Epub 2013 Apr 26.
Clin Genet. 2013.
PMID: 23320472
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Parvalbumin expression and gamma oscillation occurrence increase over time in a neurodevelopmental model of NMDA receptor dysfunction.
van Lier B, Hierlemann A, Knoflach F.
van Lier B, et al.
PeerJ. 2018 Sep 19;6:e5543. doi: 10.7717/peerj.5543. eCollection 2018.
PeerJ. 2018.
PMID: 30258707
Free PMC article.
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Pteridine regulation of inhibition of hepatic uroporphyrinogen L synthetase activity by lead chloride.
Piper WN, Van Lier BL.
Piper WN, et al. Among authors: van lier bl.
Mol Pharmacol. 1977 Nov;13(6):1126-35.
Mol Pharmacol. 1977.
PMID: 593266
No abstract available.
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