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

Year Number of Results
1952 1
1956 1
1957 8
1958 8
1959 7
1960 13
1961 28
1962 30
1964 4
1965 38
1966 86
1967 130
1968 166
1969 186
1970 220
1971 275
1972 246
1973 229
1974 326
1975 283
1976 334
1977 368
1978 334
1979 361
1980 366
1981 395
1982 395
1983 442
1984 457
1985 466
1986 405
1987 553
1988 516
1989 502
1990 614
1991 605
1992 729
1993 853
1994 818
1995 844
1996 909
1997 1017
1998 918
1999 1027
2000 1090
2001 1022
2002 948
2003 1007
2004 1024
2005 1221
2006 1222
2007 1198
2008 1274
2009 1316
2010 1481
2011 1481
2012 1484
2013 1566
2014 1526
2015 1446
2016 1421
2017 1350
2018 1318
2019 689
2020 26
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Article attribute
Article type
Publication date

Search Results

39,112 results
Results by year
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Page 1
Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
Bruel AL, Franco B, Duffourd Y, Thevenon J, Jego L, Lopez E, Deleuze JF, Doummar D, Giles RH, Johnson CA, Huynen MA, Chevrier V, Burglen L, Morleo M, Desguerres I, Pierquin G, Doray B, Gilbert-Dussardier B, Reversade B, Steichen-Gersdorf E, Baumann C, Panigrahi I, Fargeot-Espaliat A, Dieux A, David A, Goldenberg A, Bongers E, Gaillard D, Argente J, Aral B, Gigot N, St-Onge J, Birnbaum D, Phadke SR, Cormier-Daire V, Eguether T, Pazour GJ, Herranz-Pérez V, Goldstein JS, Pasquier L, Loget P, Saunier S, Mégarbané A, Rosnet O, Leroux MR, Wallingford JB, Blacque OE, Nachury MV, Attie-Bitach T, Rivière JB, Faivre L, Thauvin-Robinet C. Bruel AL, et al. J Med Genet. 2017 Jun;54(6):371-380. doi: 10.1136/jmedgenet-2016-104436. Epub 2017 Mar 13. J Med Genet. 2017. PMID: 28289185 Free PMC article. Review.
Prenatal reflex DNA screening for trisomy 21, 18 and 13.
Wald NJ. Wald NJ. Expert Rev Mol Diagn. 2018 May;18(5):399-401. doi: 10.1080/14737159.2018.1462703. Epub 2018 Apr 24. Expert Rev Mol Diagn. 2018. PMID: 29633889 Review. No abstract available.
Syndromes associated with holoprosencephaly.
Kruszka P, Muenke M. Kruszka P, et al. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):229-237. doi: 10.1002/ajmg.c.31620. Epub 2018 May 17. Am J Med Genet C Semin Med Genet. 2018. PMID: 29770994 Free PMC article.
Commentary.
Tan WH. Tan WH. Clin Chem. 2015 Jan;61(1):54. doi: 10.1373/clinchem.2014.232934. Clin Chem. 2015. PMID: 25550476 No abstract available.
Preface.
Dierssen M, de la Torre R. Dierssen M, et al. Prog Brain Res. 2012;197:vii. doi: 10.1016/B978-0-444-54299-1.00019-4. Prog Brain Res. 2012. PMID: 22541297 No abstract available.
Commentary.
Butler MG. Butler MG. Clin Chem. 2015 Jan;61(1):55. doi: 10.1373/clinchem.2014.232942. Clin Chem. 2015. PMID: 25550477 No abstract available.
Digynic triploidy in a fetus presenting with semilobar holoprosencephaly.
Chuang TY, Chang SY, Chen CP, Lin MH, Chen CY, Chen SW, Chern SR, Lee CC, Town DD, Wang W. Chuang TY, et al. Taiwan J Obstet Gynecol. 2018 Dec;57(6):881-884. doi: 10.1016/j.tjog.2018.11.001. Taiwan J Obstet Gynecol. 2018. PMID: 30545546 Free article.
The role of imprinted genes in humans.
Ishida M, Moore GE. Ishida M, et al. Mol Aspects Med. 2013 Jul-Aug;34(4):826-40. doi: 10.1016/j.mam.2012.06.009. Epub 2012 Jul 4. Mol Aspects Med. 2013. PMID: 22771538 Free article. Review.
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