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

Year Number of Results
1986 1
1989 1
1990 6
1991 10
1992 7
1993 5
1994 4
1995 7
1996 7
1997 5
1998 4
1999 2
2000 5
2001 6
2002 4
2003 4
2004 7
2005 3
2006 12
2007 10
2008 8
2009 9
2010 8
2011 11
2012 11
2013 10
2014 10
2015 9
2016 7
2017 2
2018 2
2019 5
2020 5
2021 5
2022 1
2023 6
2024 1
2025 0

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199 results

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Page 1
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Bonadona V, Bonaïti B, Olschwang S, Grandjouan S, Huiart L, Longy M, Guimbaud R, Buecher B, Bignon YJ, Caron O, Colas C, Noguès C, Lejeune-Dumoulin S, Olivier-Faivre L, Polycarpe-Osaer F, Nguyen TD, Desseigne F, Saurin JC, Berthet P, Leroux D, Duffour J, Manouvrier S, Frébourg T, Sobol H, Lasset C, Bonaïti-Pellié C; French Cancer Genetics Network. Bonadona V, et al. JAMA. 2011 Jun 8;305(22):2304-10. doi: 10.1001/jama.2011.743. JAMA. 2011. PMID: 21642682
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.
Micol R, Ben Slama L, Suarez F, Le Mignot L, Beauté J, Mahlaoui N, Dubois d'Enghien C, Laugé A, Hall J, Couturier J, Vallée L, Delobel B, Rivier F, Nguyen K, Billette de Villemeur T, Stephan JL, Bordigoni P, Bertrand Y, Aladjidi N, Pedespan JM, Thomas C, Pellier I, Koenig M, Hermine O, Picard C, Moshous D, Neven B, Lanternier F, Blanche S, Tardieu M, Debré M, Fischer A, Stoppa-Lyonnet D; CEREDIH Network Investigators. Micol R, et al. J Allergy Clin Immunol. 2011 Aug;128(2):382-9.e1. doi: 10.1016/j.jaci.2011.03.052. Epub 2011 Jun 12. J Allergy Clin Immunol. 2011. PMID: 21665257
[Medical genetics].
Jonveaux P. Jonveaux P. Pathol Biol (Paris). 2010 Oct;58(5):315. doi: 10.1016/j.patbio.2010.08.005. Epub 2010 Sep 15. Pathol Biol (Paris). 2010. PMID: 20832192 French. No abstract available.
Clonal chromosome abnormalities in Fanconi anemia.
Berger R, Jonveaux P. Berger R, et al. Among authors: jonveaux p. Hematol Cell Ther. 1996 Aug;38(4):291-6. doi: 10.1007/s00282-996-0291-6. Hematol Cell Ther. 1996. PMID: 8891720 Review.
Delineation of 15q13.3 microdeletions.
Masurel-Paulet A, Andrieux J, Callier P, Cuisset JM, Le Caignec C, Holder M, Thauvin-Robinet C, Doray B, Flori E, Alex-Cordier MP, Beri M, Boute O, Delobel B, Dieux A, Vallee L, Jaillard S, Odent S, Isidor B, Beneteau C, Vigneron J, Bilan F, Gilbert-Dussardier B, Dubourg C, Labalme A, Bidon C, Gautier A, Pernes P, Pinoit JM, Huet F, Mugneret F, Aral B, Jonveaux P, Sanlaville D, Faivre L. Masurel-Paulet A, et al. Among authors: jonveaux p. Clin Genet. 2010 Aug;78(2):149-61. doi: 10.1111/j.1399-0004.2010.01374.x. Epub 2010 Feb 9. Clin Genet. 2010. PMID: 20236110
[Cytogenetics 2008 and pathologie et biologie].
Berger R, Jonveaux P. Berger R, et al. Among authors: jonveaux p. Pathol Biol (Paris). 2008 Sep;56(6):343-4. doi: 10.1016/j.patbio.2008.03.014. Epub 2008 Jun 2. Pathol Biol (Paris). 2008. PMID: 18513890 French. No abstract available.
Terminal deletion of the long arm of chromosome 10.
Scigliano S, Grégoire MJ, Schmitt M, Jonveaux PH, LeHeup B. Scigliano S, et al. Among authors: jonveaux ph. Clin Genet. 2004 Apr;65(4):294-8. doi: 10.1111/j.1399-0004.2004.00218.x. Clin Genet. 2004. PMID: 15025722 Review.
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management].
Frebourg T, Abel A, Bonaiti-Pellie C, Brugières L, Berthet P, Bressac-de Paillerets B, Chevrier A, Chompret A, Cohen-Haguenauer O, Delattre O, Feingold J, Feunteun J, Frappaz D, Fricker JP, Gesta P, Jonveaux P, Kalifa C, Lasset C, Leheup B, Limacher JM, Longy M, Nogues C, Oppenheim D, Sommelet D, Soubrier F, Stoll C, Stoppa-Lyonnet D, Tristant H. Frebourg T, et al. Among authors: jonveaux p. Bull Cancer. 2001 Jun;88(6):581-7. Bull Cancer. 2001. PMID: 11459705 Free article. Review. French.
199 results