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

Year Number of Results
1948 1
1951 1
1952 1
1955 1
1960 1
1980 1
1982 1
1983 1
1984 3
1986 5
1987 2
1988 5
1989 3
1990 2
1992 5
1993 1
1994 6
1995 7
1996 4
1997 7
1998 2
1999 4
2000 2
2001 6
2002 5
2003 3
2004 2
2005 2
2006 2
2007 1
2008 4
2009 4
2010 7
2011 11
2012 6
2013 13
2014 14
2015 11
2016 9
2017 8
2018 9
2019 12
2020 1
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 28484071

185 results
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Page 1
The "New Genetics" in Clinical Practice: A Brief Primer.
Milunsky A. Milunsky A. J Am Board Fam Med. 2017 May-Jun;30(3):377-379. doi: 10.3122/jabfm.2017.03.160316. J Am Board Fam Med. 2017. PMID: 28484071 Free article. Review.
[Medical genetics and the genome].
Gerdes AM, Vogel I. Gerdes AM, et al. Ugeskr Laeger. 2014 Nov 10;176(46):V06140361. Ugeskr Laeger. 2014. PMID: 25394930 Review. Danish.
Carrier testing in children and adolescents.
Vears DF, Metcalfe SA. Vears DF, et al. Eur J Med Genet. 2015 Dec;58(12):659-67. doi: 10.1016/j.ejmg.2015.11.006. Epub 2015 Nov 10. Eur J Med Genet. 2015. PMID: 26563495 Review.
Unlocking Mendelian disease using exome sequencing.
Gilissen C, Hoischen A, Brunner HG, Veltman JA. Gilissen C, et al. Genome Biol. 2011 Sep 14;12(9):228. doi: 10.1186/gb-2011-12-9-228. Genome Biol. 2011. PMID: 21920049 Free PMC article. Review.
Molecular findings among patients referred for clinical whole-exome sequencing.
Yang Y, Muzny DM, Xia F, Niu Z, Person R, Ding Y, Ward P, Braxton A, Wang M, Buhay C, Veeraraghavan N, Hawes A, Chiang T, Leduc M, Beuten J, Zhang J, He W, Scull J, Willis A, Landsverk M, Craigen WJ, Bekheirnia MR, Stray-Pedersen A, Liu P, Wen S, Alcaraz W, Cui H, Walkiewicz M, Reid J, Bainbridge M, Patel A, Boerwinkle E, Beaudet AL, Lupski JR, Plon SE, Gibbs RA, Eng CM. Yang Y, et al. JAMA. 2014 Nov 12;312(18):1870-9. doi: 10.1001/jama.2014.14601. JAMA. 2014. PMID: 25326635 Free PMC article. Clinical Trial.
Rapid whole genome sequencing and precision neonatology.
Petrikin JE, Willig LK, Smith LD, Kingsmore SF. Petrikin JE, et al. Semin Perinatol. 2015 Dec;39(8):623-31. doi: 10.1053/j.semperi.2015.09.009. Epub 2015 Oct 29. Semin Perinatol. 2015. PMID: 26521050 Free PMC article. Review.
Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.
van den Veyver IB, Eng CM. van den Veyver IB, et al. Cold Spring Harb Perspect Med. 2015 Aug 7;5(10):a023077. doi: 10.1101/cshperspect.a023077. Cold Spring Harb Perspect Med. 2015. PMID: 26253094 Free PMC article. Review.
Preimplantation diagnosis of genetic diseases.
Adiga SK, Kalthur G, Kumar P, Girisha KM. Adiga SK, et al. J Postgrad Med. 2010 Oct-Dec;56(4):317-20. doi: 10.4103/0022-3859.70943. J Postgrad Med. 2010. PMID: 20935409 Free article. Review.
[Diagnostics in human genetics : Integration of phenotypic and genomic data].
Köhler S, Robinson PN. Köhler S, et al. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2017 May;60(5):542-549. doi: 10.1007/s00103-017-2538-5. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2017. PMID: 28293716 German.
Whole Exome Sequencing: Applications in Prenatal Genetics.
Jelin AC, Vora N. Jelin AC, et al. Obstet Gynecol Clin North Am. 2018 Mar;45(1):69-81. doi: 10.1016/j.ogc.2017.10.003. Obstet Gynecol Clin North Am. 2018. PMID: 29428287 Free PMC article. Review.
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