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

Year Number of Results
1974 1
1976 1
1977 1
1978 4
1979 2
1980 1
1981 2
1982 3
1984 2
1986 1
1987 4
1988 2
1990 2
1991 1
1992 5
1993 1
1995 2
1996 1
1997 4
1998 1
1999 9
2000 9
2001 5
2002 5
2003 8
2004 5
2005 4
2006 2
2007 4
2008 7
2009 10
2010 7
2011 9
2012 6
2013 10
2014 7
2015 2
2016 5
2017 3
2018 1
2020 1
2021 3
2025 0

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154 results

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Page 1
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations.
Lepri F, De Luca A, Stella L, Rossi C, Baldassarre G, Pantaleoni F, Cordeddu V, Williams BJ, Dentici ML, Caputo V, Venanzi S, Bonaguro M, Kavamura I, Faienza MF, Pilotta A, Stanzial F, Faravelli F, Gabrielli O, Marino B, Neri G, Silengo MC, Ferrero GB, Torrrente I, Selicorni A, Mazzanti L, Digilio MC, Zampino G, Dallapiccola B, Gelb BD, Tartaglia M. Lepri F, et al. Among authors: silengo mc. Hum Mutat. 2011 Jul;32(7):760-72. doi: 10.1002/humu.21492. Epub 2011 Apr 28. Hum Mutat. 2011. PMID: 21387466 Free PMC article.
Ectodermal abnormalities in Kabuki syndrome.
Lerone M, Priolo M, Naselli A, Vignolo M, Romeo G, Silengo MC. Lerone M, et al. Among authors: silengo mc. Am J Med Genet. 1997 Dec 19;73(3):263-6. doi: 10.1002/(sici)1096-8628(19971219)73:3<263::aid-ajmg6>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9415681 Review.
Ectodermal dysplasias: not only 'skin' deep.
Priolo M, Silengo M, Lerone M, Ravazzolo R. Priolo M, et al. Among authors: silengo m. Clin Genet. 2000 Dec;58(6):415-30. doi: 10.1034/j.1399-0004.2000.580601.x. Clin Genet. 2000. PMID: 11149610 Review.
Fetal growth patterns in Beckwith-Wiedemann syndrome.
Mussa A, Russo S, de Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Silengo MC, Larizza L, Riccio A, Ferrero GB. Mussa A, et al. Among authors: silengo mc. Clin Genet. 2016 Jul;90(1):21-7. doi: 10.1111/cge.12759. Epub 2016 Mar 15. Clin Genet. 2016. PMID: 26857110
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?
Bohring A, Silengo M, Lerone M, Superneau DW, Spaich C, Braddock SR, Poss A, Opitz JM. Bohring A, et al. Among authors: silengo m. Am J Med Genet. 1999 Aug 27;85(5):438-46. doi: 10.1002/(sici)1096-8628(19990827)85:5<438::aid-ajmg2>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10405439 Review.
Schinzel-Giedion syndrome with sacrococcygeal teratoma.
Sandri A, Manazza AD, Bertin D, Silengo M, Basso ME, Forni M, Madon E. Sandri A, et al. Among authors: silengo m. J Pediatr Hematol Oncol. 2003 Jul;25(7):558-61. doi: 10.1097/00043426-200307000-00012. J Pediatr Hematol Oncol. 2003. PMID: 12847324
[Genetic aspects of the adrenogenital syndrome].
Franceschini P, Silengo M. Franceschini P, et al. Among authors: silengo m. Minerva Endocrinol. 1987 Apr-Jun;12(2):85-96. Minerva Endocrinol. 1987. PMID: 3302651 Review. Italian. No abstract available.
154 results