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

Year Number of Results
1961 1
1966 1
1970 3
1971 2
1972 3
1973 4
1974 2
1976 2
1977 1
1978 2
1979 3
1980 6
1981 3
1982 1
1984 1
1985 1
1987 1
1988 1
1990 1
1991 1
1997 1
1998 3
1999 3
2000 3
2001 1
2002 3
2003 5
2004 1
2006 2
2007 2
2008 4
2009 3
2010 5
2011 3
2012 9
2013 11
2014 14
2015 18
2016 17
2017 14
2018 7
2019 5
2020 9
2021 13
2022 0
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Search Results

176 results
Results by year
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Page 1
Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variants.
Zhang LX, Lemire G, Gonzaga-Jauregui C, Molidperee S, Galaz-Montoya C, Liu DS, Verloes A, Shillington AG, Izumi K, Ritter AL, Keena B, Zackai E, Li D, Bhoj E, Tarpinian JM, Bedoukian E, Kukolich MK, Innes AM, Ediae GU, Sawyer SL, Nair KM, Soumya PC, Subbaraman KR, Probst FJ, Bassetti JA, Sutton RV, Gibbs RA, Brown C, Boone PM, Holm IA, Tartaglia M, Ferrero GB, Niceta M, Dentici ML, Radio FC, Keren B, Wells CF, Coubes C, Laquerrière A, Aziza J, Dubucs C, Nampoothiri S, Mowat D, Patel MS, Bracho A, Cammarata-Scalisi F, Gezdirici A, Fernandez-Jaen A, Hauser N, Zarate YA, Bosanko KA, Dieterich K, Carey JC, Chong JX, Nickerson DA, Bamshad MJ, Lee BH, Yang XJ, Lupski JR, Campeau PM. Zhang LX, et al. Among authors: probst fj. Genet Med. 2020 Aug;22(8):1338-1347. doi: 10.1038/s41436-020-0811-8. Epub 2020 May 19. Genet Med. 2020. PMID: 32424177 Free PMC article. Review.
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.
Reijnders MR, Zachariadis V, Latour B, Jolly L, Mancini GM, Pfundt R, Wu KM, van Ravenswaaij-Arts CM, Veenstra-Knol HE, Anderlid BM, Wood SA, Cheung SW, Barnicoat A, Probst F, Magoulas P, Brooks AS, Malmgren H, Harila-Saari A, Marcelis CM, Vreeburg M, Hobson E, Sutton VR, Stark Z, Vogt J, Cooper N, Lim JY, Price S, Lai AH, Domingo D, Reversade B; DDD Study, Gecz J, Gilissen C, Brunner HG, Kini U, Roepman R, Nordgren A, Kleefstra T. Reijnders MR, et al. Among authors: probst f. Am J Hum Genet. 2016 Feb 4;98(2):373-81. doi: 10.1016/j.ajhg.2015.12.015. Epub 2016 Jan 28. Am J Hum Genet. 2016. PMID: 26833328 Free PMC article.
Letter to the editor.
Schiel S, Mayer P, Probst FA, Otto S, Cornelius CP. Schiel S, et al. Among authors: probst fa. J Oral Maxillofac Surg. 2014 Feb;72(2):237-8. doi: 10.1016/j.joms.2013.10.007. Epub 2013 Nov 23. J Oral Maxillofac Surg. 2014. PMID: 24280173 Free article. No abstract available.
Confidentiality.
Probst F. Probst F. J R Soc Med. 2002 Apr;95(4):218-9; author reply 219. doi: 10.1258/jrsm.95.4.218-c. J R Soc Med. 2002. PMID: 11934921 Free PMC article. No abstract available.
Spontaneous tension haemopneumothorax.
Patterson BO, Itam S, Probst F. Patterson BO, et al. Among authors: probst f. Scand J Trauma Resusc Emerg Med. 2008 Oct 31;16:12. doi: 10.1186/1757-7241-16-12. Scand J Trauma Resusc Emerg Med. 2008. PMID: 18976471 Free PMC article.
[Calvarial reconstruction by customized bioactive implant].
Probst FA, Hutmacher DW, Müller DF, Machens HG, Schantz JT. Probst FA, et al. Handchir Mikrochir Plast Chir. 2010 Dec;42(6):369-73. doi: 10.1055/s-0030-1248310. Epub 2010 Mar 10. Handchir Mikrochir Plast Chir. 2010. PMID: 20221990 Review. German.
Urinary tract infection.
Hoey R, Probst F. Hoey R, et al. Among authors: probst f. N Engl J Med. 2003 Oct 23;349(17):1674-6; author reply 1674-6. N Engl J Med. 2003. PMID: 14575059 No abstract available.
[Unclear massive hemorrhage with obstruction of the airways].
Brunner T, Möhnle P, Probst F, Welz C, Ehrenfeld M, Ney L. Brunner T, et al. Among authors: probst f. HNO. 2021 Dec;69(12):1009-1011. doi: 10.1007/s00106-021-01025-0. Epub 2021 Mar 15. HNO. 2021. PMID: 33723671 German. No abstract available.
176 results