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

Year Number of Results
1998 3
1999 1
2000 4
2001 7
2002 4
2003 4
2005 1
2006 1
2009 1
2010 3
2011 5
2012 3
2014 1
2015 3
2016 4
2017 5
2018 3
2019 5
2020 12
2021 17
2022 11
2023 5

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91 results

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Page 1
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Chopra M, McEntagart M, Clayton-Smith J, Platzer K, Shukla A, Girisha KM, Kaur A, Kaur P, Pfundt R, Veenstra-Knol H, Mancini GMS, Cappuccio G, Brunetti-Pierri N, Kortüm F, Hempel M, Denecke J, Lehman A; CAUSES Study; Kleefstra T, Stuurman KE, Wilke M, Thompson ML, Bebin EM, Bijlsma EK, Hoffer MJV, Peeters-Scholte C, Slavotinek A, Weiss WA, Yip T, Hodoglugil U, Whittle A, diMonda J, Neira J, Yang S, Kirby A, Pinz H, Lechner R, Sleutels F, Helbig I, McKeown S, Helbig K, Willaert R, Juusola J, Semotok J, Hadonou M, Short J; Genomics England Research Consortium; Yachelevich N, Lala S, Fernández-Jaen A, Pelayo JP, Klöckner C, Kamphausen SB, Abou Jamra R, Arelin M, Innes AM, Niskakoski A, Amin S, Williams M, Evans J, Smithson S, Smedley D, de Burca A, Kini U, Delatycki MB, Gallacher L, Yeung A, Pais L, Field M, Martin E, Charles P, Courtin T, Keren B, Iascone M, Cereda A, Poke G, Abadie V, Chalouhi C, Parthasarathy P, Halliday BJ, Robertson SP, Lyonnet S, Amiel J, Gordon CT. Chopra M, et al. Among authors: klockner c. Am J Hum Genet. 2021 Jun 3;108(6):1138-1150. doi: 10.1016/j.ajhg.2021.04.007. Epub 2021 Apr 27. Am J Hum Genet. 2021. PMID: 33909992 Free PMC article.
[Polysegmental Dynesys system].
Klöckner C, Beck A. Klöckner C, et al. Orthopade. 2011 Feb;40(2):156-61. doi: 10.1007/s00132-010-1715-0. Orthopade. 2011. PMID: 21308463 Clinical Trial. German.
Genetic and phenotypic spectrum in the NONO-associated syndromic disorder.
Roessler F, Beck AE, Susie B, Tobias B, Begtrup A, Biskup S, Caluseriu O, Delanty N, Fröhlich C, Greally MT, Karnstedt M, Klöckner C, Kurtzberg J, Schubert S, Schulze M, Weidenbach M, Westphal DS, White M, Wolf CM, Zyskind J, Popp B, Strehlow V. Roessler F, et al. Among authors: klockner c. Am J Med Genet A. 2023 Feb;191(2):469-478. doi: 10.1002/ajmg.a.63044. Epub 2022 Nov 25. Am J Med Genet A. 2023. PMID: 36426740 Review.
[Obese, fat or just overweight?].
Strømmen M, Bakken IJ, Andenæs E, Klöckner CA, Mårvik R, Kulseng B, Holen A. Strømmen M, et al. Among authors: klockner ca. Tidsskr Nor Laegeforen. 2015 Nov 3;135(20):1816. doi: 10.4045/tidsskr.15.1095. eCollection 2015 Nov 3. Tidsskr Nor Laegeforen. 2015. PMID: 26534804 Free article. Norwegian. No abstract available.
Obese, fat, or just overweight?
Strømmen M, Bakken IJ, Andenæs E, Klöckner CA, Mårvik R, Kulseng B, Holen A. Strømmen M, et al. Among authors: klockner ca. Tidsskr Nor Laegeforen. 2015 Oct 20;135(19):1732-6. doi: 10.4045/tidsskr.14.0828. eCollection 2015 Oct 20. Tidsskr Nor Laegeforen. 2015. PMID: 26486667 Free article. English, Norwegian.
91 results