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

Year Number of Results
1946 3
1947 2
1948 7
1949 1
1951 20
1952 35
1953 42
1954 45
1955 31
1956 59
1957 75
1958 55
1959 54
1960 91
1961 100
1962 64
1963 3
1964 18
1965 199
1966 436
1967 497
1968 560
1969 581
1970 613
1971 634
1972 724
1973 682
1974 717
1975 678
1976 689
1977 766
1978 759
1979 749
1980 689
1981 766
1982 853
1983 820
1984 805
1985 814
1986 846
1987 951
1988 907
1989 956
1990 1077
1991 1093
1992 1157
1993 1204
1994 1086
1995 1206
1996 1220
1997 1250
1998 1489
1999 1614
2000 1567
2001 1596
2002 1653
2003 1792
2004 1890
2005 2065
2006 2388
2007 2354
2008 2571
2009 2534
2010 2883
2011 3273
2012 3361
2013 3771
2014 3978
2015 3878
2016 3974
2017 3988
2018 3877
2019 2186
2020 83
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80,571 results
Results by year
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Page 1
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, Breman A, Xia F, Yang Y, Purgason A, Pourpak A, Chen Z, Wang X, Wang Y, Kulkarni S, Choy KW, Wapner RJ, Van den Veyver IB, Beaudet A, Parmar S, Wong LJ, Eng CM. Zhang J, et al. Nat Med. 2019 Mar;25(3):439-447. doi: 10.1038/s41591-018-0334-x. Epub 2019 Jan 28. Nat Med. 2019. PMID: 30692697
Hereditary Tumor Syndromes with Skin Involvement.
Hamid RN, Akkurt ZM. Hamid RN, et al. Dermatol Clin. 2019 Oct;37(4):607-613. doi: 10.1016/j.det.2019.05.016. Epub 2019 Jul 30. Dermatol Clin. 2019. PMID: 31466598 Review.
Molecular diagnosis of genetic diseases.
Fong CT. Fong CT. Pediatr Ann. 1993 May;22(5):304-10. doi: 10.3928/0090-4481-19930501-10. Pediatr Ann. 1993. PMID: 8390046 Review. No abstract available.
Clinical diagnosis of genetic diseases.
Fong CT. Fong CT. Pediatr Ann. 1993 May;22(5):277-81. doi: 10.3928/0090-4481-19930501-07. Pediatr Ann. 1993. PMID: 8510994 Review. No abstract available.
Lyonization in ophthalmology.
Wuthisiri W, Lingao MD, Capasso JE, Levin AV. Wuthisiri W, et al. Curr Opin Ophthalmol. 2013 Sep;24(5):389-97. doi: 10.1097/ICU.0b013e3283641f91. Curr Opin Ophthalmol. 2013. PMID: 23892913 Review.
Unusual Presentations of Dystrophinopathies in Childhood.
Allen NM, Ewer A, Nakou V, Konstantoulaki E, Wraige E, Gowda V, Jungbluth H. Allen NM, et al. Pediatrics. 2018 Apr;141(Suppl 5):S510-S514. doi: 10.1542/peds.2017-2391. Pediatrics. 2018. PMID: 29610182 Free article.
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