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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2012 2
2014 2
2015 5
2016 2
2021 0
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11 results
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Page 1
Lactotransferrin Gene Polymorphism Associated with Caries Experience.
Doetzer AD, Brancher JA, Pecharki GD, Schlipf N, Werneck R, Mira MT, Riess O, Bauer P, Trevilatto PC. Doetzer AD, et al. Among authors: schlipf n. Caries Res. 2015;49(4):370-7. doi: 10.1159/000366211. Epub 2015 May 13. Caries Res. 2015. PMID: 25998152
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes.
Dufke C, Schlipf N, Schüle R, Bonin M, Auer-Grumbach M, Stevanin G, Depienne C, Kassubek J, Klebe S, Klimpe S, Klopstock T, Otto S, Poths S, Seibel A, Stolze H, Gal A, Schöls L, Bauer P. Dufke C, et al. Among authors: schlipf n. Neurogenetics. 2012 Aug;13(3):215-27. doi: 10.1007/s10048-012-0329-6. Epub 2012 May 3. Neurogenetics. 2012. PMID: 22552817
Large deletions in the NSDHL gene in two patients with CHILD syndrome.
Yang Z, Hartmann B, Xu Z, Ma L, Happle R, Schlipf N, Zhang LX, Xu ZG, Wang ZY, Fischer J. Yang Z, et al. Among authors: schlipf n. Acta Derm Venereol. 2015 Nov;95(8):1007-8. doi: 10.2340/00015555-2143. Acta Derm Venereol. 2015. PMID: 26014843 Free article. No abstract available.
11 results