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Year | Number of Results |
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1997 | 1 |
1999 | 1 |
2002 | 2 |
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2024 | 0 |
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Page 1
Further delineation of the chromosome 14q terminal deletion syndrome.
Am J Med Genet. 2002 Jun 1;110(1):65-72. doi: 10.1002/ajmg.10207.
Am J Med Genet. 2002.
PMID: 12116274
Review.
New Generation of Mesoporous Silica Membranes Prepared by a Stöber-Solution Pore-Growth Approach.
Pizzoccaro-Zilamy MA, Huiskes C, Keim EG, Sluijter SN, van Veen H, Nijmeijer A, Winnubst L, Luiten-Olieman MWJ.
Pizzoccaro-Zilamy MA, et al. Among authors: sluijter sn.
ACS Appl Mater Interfaces. 2019 May 22;11(20):18528-18539. doi: 10.1021/acsami.9b03526. Epub 2019 May 13.
ACS Appl Mater Interfaces. 2019.
PMID: 31038910
Free PMC article.
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Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.
van Karnebeek CD, Koevoets C, Sluijter S, Bijlsma EK, Smeets DF, Redeker EJ, Hennekam RC, Hoovers JM.
van Karnebeek CD, et al. Among authors: sluijter s.
J Med Genet. 2002 Aug;39(8):546-53. doi: 10.1136/jmg.39.8.546.
J Med Genet. 2002.
PMID: 12161591
Free PMC article.
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Synthesis of palladium(0) and -(II) complexes with chelating bis(N-heterocyclic carbene) ligands and their application in semihydrogenation.
Sluijter SN, Warsink S, Lutz M, Elsevier CJ.
Sluijter SN, et al.
Dalton Trans. 2013 May 28;42(20):7365-72. doi: 10.1039/c3dt32835j.
Dalton Trans. 2013.
PMID: 23380807
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Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?
Aalfs CM, Fantes JA, Wenniger-Prick LJ, Sluijter S, Hennekam RC, van Heyningen V, Hoovers JM.
Aalfs CM, et al. Among authors: sluijter s.
Am J Med Genet. 1997 Dec 19;73(3):267-71. doi: 10.1002/(sici)1096-8628(19971219)73:3<267::aid-ajmg7>3.0.co;2-p.
Am J Med Genet. 1997.
PMID: 9415682
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A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).
Mohrschladt MF, Bijlsma EK, Sluijter S, De Coo RF, Hoovers JM, Leschot NJ.
Mohrschladt MF, et al. Among authors: sluijter s.
Clin Dysmorphol. 1999 Jul;8(3):211-4.
Clin Dysmorphol. 1999.
PMID: 10457857
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