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

Year Number of Results
1946 2
1947 2
1948 3
1950 7
1951 8
1952 5
1953 5
1954 11
1955 14
1956 13
1957 15
1958 4
1959 9
1960 5
1961 9
1962 5
1963 11
1964 14
1965 2
1966 1
1967 6
1968 12
1969 11
1970 11
1971 9
1972 10
1973 12
1974 14
1975 25
1976 15
1977 17
1978 13
1979 11
1980 16
1981 25
1982 14
1983 14
1984 25
1985 26
1986 20
1987 26
1988 24
1989 26
1990 39
1991 34
1992 52
1993 41
1994 45
1995 44
1996 50
1997 62
1998 77
1999 68
2000 60
2001 41
2002 64
2003 52
2004 62
2005 55
2006 59
2007 75
2008 87
2009 73
2010 83
2011 104
2012 111
2013 101
2014 132
2015 143
2016 118
2017 114
2018 124
2019 69
2020 2
Text availability
Article attribute
Article type
Publication date

Search Results

2,561 results
Results by year
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Page 1
Homozygous.D.
Contreras M, Armitage S, Daniels GL, Tippett P. Contreras M, et al. Vox Sang. 1979;36(2):81-4. doi: 10.1111/j.1423-0410.1979.tb04403.x. Vox Sang. 1979. PMID: 111421
CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder.
Finsterer J, Fiorini AC, Scorza CA, Scorza FA. Finsterer J, et al. Eur J Paediatr Neurol. 2018 Sep;22(5):889-891. doi: 10.1016/j.ejpn.2018.04.012. Epub 2018 Apr 30. Eur J Paediatr Neurol. 2018. PMID: 29752145 No abstract available.
Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis.
Zhang D, Zhou Z, Abu-Hijleh M, Batra K, Xing C, Garcia CK. Zhang D, et al. Am J Respir Crit Care Med. 2019 Mar 15;199(6):797-799. doi: 10.1164/rccm.201809-1632LE. Am J Respir Crit Care Med. 2019. PMID: 30525901 Free PMC article. No abstract available.
Runs of homozygosity: current knowledge and applications in livestock.
Peripolli E, Munari DP, Silva MVGB, Lima ALF, Irgang R, Baldi F. Peripolli E, et al. Anim Genet. 2017 Jun;48(3):255-271. doi: 10.1111/age.12526. Epub 2016 Dec 1. Anim Genet. 2017. PMID: 27910110 Review.
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