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Page 1
Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases.
Tessier A, Sarreau M, Pelluard F, André G, Blesson S, Bucourt M, Dechelotte P, Faivre L, Frébourg T, Goldenberg A, Goua V, Jeanne-Pasquier C, Guimiot F, Laquerriere A, Laurent N, Lefebvre M, Loget P, Maréchaud M, Mechler C, Perez MJ, Sabourin JC, Verloes A, Patrier S, Guerrot AM. Tessier A, et al. Among authors: dechelotte p. Prenat Diagn. 2016 Dec;36(13):1270-1275. doi: 10.1002/pd.4971. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27859469 Review.
Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
Madariaga L, Morinière V, Jeanpierre C, Bouvier R, Loget P, Martinovic J, Dechelotte P, Leporrier N, Thauvin-Robinet C, Jensen UB, Gaillard D, Mathieu M, Turlin B, Attie-Bitach T, Salomon R, Gübler MC, Antignac C, Heidet L. Madariaga L, et al. Among authors: dechelotte p. Clin J Am Soc Nephrol. 2013 Jul;8(7):1179-87. doi: 10.2215/CJN.10221012. Epub 2013 Mar 28. Clin J Am Soc Nephrol. 2013. PMID: 23539225 Free PMC article.
Extending the ALDH18A1 clinical spectrum to severe autosomal recessive fetal cutis laxa with corpus callosum agenesis.
Lefebvre M, Beaufrere AM, Francannet C, Laurichesse H, Poe C, Jouan T, Troude B, Dechelotte P, Vabres P, Briard M, Mosca-Boidron AL, Duffourd Y, Faivre L, Thevenon J, Thauvin-Robinet C. Lefebvre M, et al. Among authors: dechelotte p. Am J Med Genet A. 2018 Nov;176(11):2509-2512. doi: 10.1002/ajmg.a.40515. Epub 2018 Sep 23. Am J Med Genet A. 2018. PMID: 30244529 No abstract available.
Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.
Debost-Legrand A, Goumy C, Laurichesse-Delmas H, Déchelotte P, Beaufrère AM, Lémery D, Francannet C, Gallot D. Debost-Legrand A, et al. Among authors: dechelotte p. Birth Defects Res A Clin Mol Teratol. 2013 Dec;97(12):806-11. doi: 10.1002/bdra.23194. Epub 2013 Nov 6. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 24343879
Prenatal diagnosis of the VACTERL association using routine ultrasound examination.
Debost-Legrand A, Goumy C, Laurichesse-Delmas H, Déchelotte P, Perthus I, Francannet C, Lémery D, Gallot D. Debost-Legrand A, et al. Among authors: dechelotte p. Birth Defects Res A Clin Mol Teratol. 2015 Oct;103(10):880-6. doi: 10.1002/bdra.23346. Epub 2015 Jun 2. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26033534
Impact of Expert Pathologic Review of Lymphoma Diagnosis: Study of Patients From the French Lymphopath Network.
Laurent C, Baron M, Amara N, Haioun C, Dandoit M, Maynadié M, Parrens M, Vergier B, Copie-Bergman C, Fabiani B, Traverse-Glehen A, Brousse N, Copin MC, Tas P, Petrella T, Rousselet MC, Brière J, Charlotte F, Chassagne-Clement C, Rousset T, Xerri L, Moreau A, Martin A, Damotte D, Dartigues P, Soubeyran I, Peoch M, Dechelotte P, Michiels JF, de Mascarel A, Berger F, Bossard C, Arbion F, Quintin-Roué I, Picquenot JM, Patey M, Fabre B, Sevestre H, Le Naoures C, Chenard-Neu MP, Bastien C, Thiebault S, Martin L, Delage M, Filleron T, Salles G, Molina TJ, Delsol G, Brousset P, Gaulard P. Laurent C, et al. Among authors: dechelotte p. J Clin Oncol. 2017 Jun 20;35(18):2008-2017. doi: 10.1200/JCO.2016.71.2083. Epub 2017 May 1. J Clin Oncol. 2017. PMID: 28459613
Antenatal detection and impact on outcome of congenital diaphragmatic hernia: a 12-year experience in Auvergne, France.
Gallot D, Coste K, Francannet C, Laurichesse H, Boda C, Ughetto S, Vanlieferinghen P, Scheye T, Vendittelli F, Labbe A, Dechelotte PJ, Sapin V, Lemery D. Gallot D, et al. Among authors: dechelotte pj. Eur J Obstet Gynecol Reprod Biol. 2006 Apr 1;125(2):202-5. doi: 10.1016/j.ejogrb.2005.06.030. Epub 2005 Aug 15. Eur J Obstet Gynecol Reprod Biol. 2006. PMID: 16099579
467 results