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

Year Number of Results
1993 2
2007 1
2008 1
2009 3
2010 3
2011 2
2012 3
2013 2
2014 2
2015 5
2016 1
2017 2
2018 2
2019 5
2020 9
2021 3
2022 4
2023 4
2024 3

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47 results

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Page 1
Periodontal Ehlers-Danlos Syndrome.
Kapferer-Seebacher I, van Dijk FS, Zschocke J. Kapferer-Seebacher I, et al. Among authors: van dijk fs. 2021 Jul 29. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2021 Jul 29. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 34324282 Free Books & Documents. Review.
TNXB-Related Classical-Like Ehlers-Danlos Syndrome.
van Dijk FS, Ghali N, Demirdas S, Baker D. van Dijk FS, et al. 2022 Sep 15. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2022 Sep 15. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 36108117 Free Books & Documents. Review.
Pectus excavatum and carinatum.
Cobben JM, Oostra RJ, van Dijk FS. Cobben JM, et al. Among authors: van dijk fs. Eur J Med Genet. 2014 Aug;57(8):414-7. doi: 10.1016/j.ejmg.2014.04.017. Epub 2014 May 10. Eur J Med Genet. 2014. PMID: 24821303 Review.
Genetics of Osteoporosis in Children.
van Dijk FS. van Dijk FS. Endocr Dev. 2015;28:196-209. doi: 10.1159/000381046. Epub 2015 Jun 12. Endocr Dev. 2015. PMID: 26138843 Review.
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome.
Vandersteen AM, Weerakkody RA, Parry DA, Kanonidou C, Toddie-Moore DJ, Vandrovcova J, Darlay R, Santoyo-Lopez J, Meynert A; NIHR BioResource; Kazkaz H, Grahame R, Cummings C, Bartlett M, Ghali N, Brady AF, Pope FM, van Dijk FS, Cordell HJ, Aitman TJ. Vandersteen AM, et al. Among authors: van dijk fs. J Med Genet. 2024 Feb 21;61(3):232-238. doi: 10.1136/jmg-2023-109329. J Med Genet. 2024. PMID: 37813462 Free article.
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.
Huang L, Vanstone MR, Hartley T, Osmond M, Barrowman N, Allanson J, Baker L, Dabir TA, Dipple KM, Dobyns WB, Estrella J, Faghfoury H, Favaro FP, Goel H, Gregersen PA, Gripp KW, Grix A, Guion-Almeida ML, Harr MH, Hudson C, Hunter AG, Johnson J, Joss SK, Kimball A, Kini U, Kline AD, Lauzon J, Lildballe DL, López-González V, Martinezmoles J, Meldrum C, Mirzaa GM, Morel CF, Morton JE, Pyle LC, Quintero-Rivera F, Richer J, Scheuerle AE, Schönewolf-Greulich B, Shears DJ, Silver J, Smith AC, Temple IK; UCLA Clinical Genomics Center; van de Kamp JM, van Dijk FS, Vandersteen AM, White SM, Zackai EH, Zou R; Care4Rare Canada Consortium; Bulman DE, Boycott KM, Lines MA. Huang L, et al. Among authors: van dijk fs. Hum Mutat. 2016 Feb;37(2):148-54. doi: 10.1002/humu.22924. Epub 2015 Nov 19. Hum Mutat. 2016. PMID: 26507355 Free PMC article. Review.
Fatigue in adults with Osteogenesis Imperfecta.
Harsevoort AGJ, Gooijer K, van Dijk FS, van der Grijn DAFM, Franken AAM, Dommisse AMV, Janus GJM. Harsevoort AGJ, et al. Among authors: van dijk fs. BMC Musculoskelet Disord. 2020 Jan 3;21(1):6. doi: 10.1186/s12891-019-3000-7. BMC Musculoskelet Disord. 2020. PMID: 31900144 Free PMC article.
An exemplary model of genetic counselling for highly specialised services.
Harris J, Bartlett M, Baker D, Berlin C, Bowen J, Cummings C, Fallows C, Green C, Griffin J, Julier K, Kammin T, Sehra R, Stacey C, Cobben J, Ghali N, Johnson D, Sobey G, van Dijk FS. Harris J, et al. Among authors: van dijk fs. J Community Genet. 2023 Apr;14(2):115-119. doi: 10.1007/s12687-023-00640-4. Epub 2023 Mar 9. J Community Genet. 2023. PMID: 36892793 Free PMC article. Review.
47 results