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

Year Number of Results
1974 2
1976 1
1977 1
1978 2
1981 1
1982 1
1983 1
1985 1
1986 2
1987 2
1988 1
1989 1
1990 5
1991 2
1992 2
1993 8
1994 3
1995 6
1996 1
1997 1
1998 3
2000 2
2001 1
2003 1
2004 1
2006 1
2011 1
2014 1
2024 0

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55 results

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Page 1
DFNA3.
Denoyelle F, Weil D, Levilliers J, Petit C. Denoyelle F, et al. Among authors: levilliers j. Adv Otorhinolaryngol. 2000;56:78-83. doi: 10.1159/000059086. Adv Otorhinolaryngol. 2000. PMID: 10868217 Review. No abstract available.
Kallmann syndrome.
Hardelin JP, Soussi-Yanicostas N, Ardouin O, Levilliers J, Petit C. Hardelin JP, et al. Among authors: levilliers j. Adv Otorhinolaryngol. 2000;56:268-74. doi: 10.1159/000059073. Adv Otorhinolaryngol. 2000. PMID: 10868244 Review. No abstract available.
[Hereditary deafness: molecular genetics].
Hardelin JP, Denoyelle F, Levilliers J, Simmler MC, Petit C. Hardelin JP, et al. Among authors: levilliers j. Med Sci (Paris). 2004 Mar;20(3):311-6. doi: 10.1051/medsci/2004203311. Med Sci (Paris). 2004. PMID: 15067576 Free article. Review. French.
Molecular genetics of hearing loss.
Petit C, Levilliers J, Hardelin JP. Petit C, et al. Among authors: levilliers j. Annu Rev Genet. 2001;35:589-646. doi: 10.1146/annurev.genet.35.102401.091224. Annu Rev Genet. 2001. PMID: 11700295 Review.
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C. Riahi Z, et al. Among authors: levilliers j. PLoS One. 2014 Jun 13;9(6):e99797. doi: 10.1371/journal.pone.0099797. eCollection 2014. PLoS One. 2014. PMID: 24926664 Free PMC article.
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Dodé C, Levilliers J, Dupont JM, De Paepe A, Le Dû N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, Pêcheux C, Le Tessier D, Cruaud C, Delpech M, Speleman F, Vermeulen S, Amalfitano A, Bachelot Y, Bouchard P, Cabrol S, Carel JC, Delemarre-van de Waal H, Goulet-Salmon B, Kottler ML, Richard O, Sanchez-Franco F, Saura R, Young J, Petit C, Hardelin JP. Dodé C, et al. Among authors: levilliers j. Nat Genet. 2003 Apr;33(4):463-5. doi: 10.1038/ng1122. Epub 2003 Mar 10. Nat Genet. 2003. PMID: 12627230
Xp22.3 deletions in isolated familial Kallmann's syndrome.
Hardelin JP, Levilliers J, Young J, Pholsena M, Legouis R, Kirk J, Bouloux P, Petit C, Schaison G. Hardelin JP, et al. Among authors: levilliers j. J Clin Endocrinol Metab. 1993 Apr;76(4):827-31. doi: 10.1210/jcem.76.4.8473391. J Clin Endocrinol Metab. 1993. PMID: 8473391
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.
Bonnet C, Grati M, Marlin S, Levilliers J, Hardelin JP, Parodi M, Niasme-Grare M, Zelenika D, Délépine M, Feldmann D, Jonard L, El-Amraoui A, Weil D, Delobel B, Vincent C, Dollfus H, Eliot MM, David A, Calais C, Vigneron J, Montaut-Verient B, Bonneau D, Dubin J, Thauvin C, Duvillard A, Francannet C, Mom T, Lacombe D, Duriez F, Drouin-Garraud V, Thuillier-Obstoy MF, Sigaudy S, Frances AM, Collignon P, Challe G, Couderc R, Lathrop M, Sahel JA, Weissenbach J, Petit C, Denoyelle F. Bonnet C, et al. Among authors: levilliers j. Orphanet J Rare Dis. 2011 May 11;6:21. doi: 10.1186/1750-1172-6-21. Orphanet J Rare Dis. 2011. PMID: 21569298 Free PMC article.
55 results