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

Year Number of Results
1977 1
1978 2
1979 2
1980 4
1981 2
1982 10
1983 6
1984 18
1985 10
1986 8
1987 4
1988 7
1989 1
1990 12
1991 5
1992 6
1993 3
1994 7
1995 5
1996 4
1997 6
1998 11
1999 7
2000 13
2001 6
2002 4
2003 6
2004 6
2005 13
2006 8
2007 5
2008 5
2009 5
2010 2
2011 2
2012 2
2013 3
2014 1
2015 1
2017 1
2018 1
2021 0
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Article type
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Search Results

214 results
Results by year
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Page 1
[Oligodontia].
van der Weide Y, Steen WH, Beemer FA, Bosman F. van der Weide Y, et al. Among authors: beemer fa. Ned Tijdschr Tandheelkd. 1990 Nov;97(11):455-7. Ned Tijdschr Tandheelkd. 1990. PMID: 2098662 Dutch.
Oculocerebrocutaneous syndrome.
Bleeker-Wagemakers LM, Hamel BC, Hennekam RC, Beemer FA, Oorthuys HW. Bleeker-Wagemakers LM, et al. Among authors: beemer fa. J Med Genet. 1990 Jan;27(1):69-70. doi: 10.1136/jmg.27.1.69. J Med Genet. 1990. PMID: 2407849 Free PMC article. Review. No abstract available.
[Johanson-Blizzard syndrome].
Rudnik-Schöneborn S, Keller B, Beemer FA, Pistor K, Swanenburg de Veye HF, Zerres K. Rudnik-Schöneborn S, et al. Among authors: beemer fa. Klin Padiatr. 1991 Jan-Feb;203(1):33-8. doi: 10.1055/s-2007-1025396. Klin Padiatr. 1991. PMID: 2027265 German.
Osteogenesis imperfecta in childhood: treatment strategies.
Engelbert RH, Pruijs HE, Beemer FA, Helders PJ. Engelbert RH, et al. Among authors: beemer fa. Arch Phys Med Rehabil. 1998 Dec;79(12):1590-4. doi: 10.1016/s0003-9993(98)90426-9. Arch Phys Med Rehabil. 1998. PMID: 9862306 Review.
VACTERL and hydrocephalus.
Beemer FA, Wanders RJ, Schutgens RB. Beemer FA, et al. Am J Med Genet. 1990 Nov;37(3):425-6. doi: 10.1002/ajmg.1320370325. Am J Med Genet. 1990. PMID: 2260576 No abstract available.
Isolated and contiguous glycerol kinase gene disorders: a review.
Sjarif DR, Ploos van Amstel JK, Duran M, Beemer FA, Poll-The BT. Sjarif DR, et al. Among authors: beemer fa. J Inherit Metab Dis. 2000 Sep;23(6):529-47. doi: 10.1023/a:1005660826652. J Inherit Metab Dis. 2000. PMID: 11032329 Review.
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.
Van Kuilenburg AB, Vreken P, Abeling NG, Bakker HD, Meinsma R, Van Lenthe H, De Abreu RA, Smeitink JA, Kayserili H, Apak MY, Christensen E, Holopainen I, Pulkki K, Riva D, Botteon G, Holme E, Tulinius M, Kleijer WJ, Beemer FA, Duran M, Niezen-Koning KE, Smit GP, Jakobs C, Smit LM, Van Gennip AH, et al. Van Kuilenburg AB, et al. Among authors: beemer fa. Hum Genet. 1999 Jan;104(1):1-9. doi: 10.1007/pl00008711. Hum Genet. 1999. PMID: 10071185 Review.
Familial elastosis perforans serpiginosa.
Langeveld-Wildschut EG, Toonstra J, van Vloten WA, Beemer FA. Langeveld-Wildschut EG, et al. Among authors: beemer fa. Arch Dermatol. 1993 Feb;129(2):205-7. Arch Dermatol. 1993. PMID: 7679569
214 results
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