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

Year Number of Results
1989 2
1993 2
1995 1
1996 1
1997 1
1999 5
2000 1
2002 2
2003 1
2004 1
2005 1
2007 1
2009 1
2020 1
2024 0

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21 results

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Page 1
Truncation of NHEJ1 in a patient with polymicrogyria.
Cantagrel V, Lossi AM, Lisgo S, Missirian C, Borges A, Philip N, Fernandez C, Cardoso C, Figarella-Branger D, Moncla A, Lindsay S, Dobyns WB, Villard L. Cantagrel V, et al. Among authors: lossi am. Hum Mutat. 2007 Apr;28(4):356-64. doi: 10.1002/humu.20450. Hum Mutat. 2007. PMID: 17191205
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome.
Villard L, Bonino MC, Abidi F, Ragusa A, Belougne J, Lossi AM, Seaver L, Bonnefont JP, Romano C, Fichera M, Lacombe D, Hanauer A, Philip N, Schwartz C, Fontés M. Villard L, et al. Among authors: lossi am. J Med Genet. 1999 Mar;36(3):183-6. J Med Genet. 1999. PMID: 10204841 Free PMC article.
Baseline ECG Features and Arrhythmic Profile in Transthyretin Versus Light Chain Cardiac Amyloidosis.
Cappelli F, Vignini E, Martone R, Perlini S, Mussinelli R, Sabena A, Morini S, Gabriele M, Taborchi G, Bartolini S, Lossi A, Nardi G, Marchionni N, Di Mario C, Olivotto I, Perfetto F. Cappelli F, et al. Among authors: lossi a. Circ Heart Fail. 2020 Mar;13(3):e006619. doi: 10.1161/CIRCHEARTFAILURE.119.006619. Epub 2020 Mar 13. Circ Heart Fail. 2020. PMID: 32164434 No abstract available.
Mutation screening of the PKD1 transcript by RT-PCR.
Burtey S, Lossi AM, Bayle J, Berland Y, Fontés M. Burtey S, et al. Among authors: lossi am. J Med Genet. 2002 Jun;39(6):422-9. doi: 10.1136/jmg.39.6.422. J Med Genet. 2002. PMID: 12070253 Free PMC article. No abstract available.
21 results