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Results by year

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

Year Number of Results
1975 4
1977 2
1978 1
1979 3
1980 1
1981 2
1982 1
1983 2
1984 5
1985 4
1986 4
1987 2
1988 1
1989 3
1990 2
1991 6
1992 11
1993 5
1994 5
1995 7
1996 7
1997 5
1998 11
1999 8
2000 3
2001 7
2002 7
2003 8
2004 8
2005 7
2006 10
2007 9
2008 10
2009 12
2010 12
2011 17
2012 17
2013 17
2014 17
2015 16
2016 17
2017 9
2018 16
2019 15
2020 26
2021 23
2022 17
2023 18
2024 6

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Publication date

PubMed for id: 98469

370 results

Results by year

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Page 1
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
Tedesco MG, Lonardo F, Ceccarini C, Cesarano C, Digilio MC, Magliozzi M, Rogaia D, Mencarelli A, Leoni C, Piscopo C, Imperatore V, Falco MT, Fontana P, Nardone AM, Novelli A, Troiani S, Seri M, Prontera P. Tedesco MG, et al. Am J Med Genet A. 2021 Apr;185(4):1204-1210. doi: 10.1002/ajmg.a.62068. Epub 2021 Jan 14. Am J Med Genet A. 2021. PMID: 33442900
Cromosoma 13 en anillo.
Cammarata-Scalisi F, Briceño Y, Cegarra E, Montilla D. Cammarata-Scalisi F, et al. Bol Med Hosp Infant Mex. 2019;76(2):100-103. doi: 10.24875/BMHIM.18000108. Bol Med Hosp Infant Mex. 2019. PMID: 30907385 English.
370 results