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Page 1
NOTCH2 related disorders: Description and review of the fetal presentation.
Deb W, Joubert M, Cogné B, Vincent M, Ghesh L, Bézieau S, Le Vaillant C, Beneteau C. Deb W, et al. Among authors: le vaillant c. Eur J Med Genet. 2023 Jul;66(7):104769. doi: 10.1016/j.ejmg.2023.104769. Epub 2023 Apr 28. Eur J Med Genet. 2023. PMID: 37121269 Review.
[Atypical oligo-arthritis].
Levaillant C, Doan C, Giard H, Liesse A, Collet B, Ganga-Zandzou PS, Pierre MH, Ythier H, Pouessel G. Levaillant C, et al. Arch Pediatr. 2011 Jun;18(6):678, 707-8. doi: 10.1016/j.arcped.2011.03.008. Epub 2011 Apr 20. Arch Pediatr. 2011. PMID: 21511445 French. No abstract available.
Prenatal sonographic findings in Peters-plus syndrome.
Boog G, Le Vaillant C, Joubert M. Boog G, et al. Among authors: le vaillant c. Ultrasound Obstet Gynecol. 2005 Jun;25(6):602-6. doi: 10.1002/uog.1910. Ultrasound Obstet Gynecol. 2005. PMID: 15912477 Free article.
[Is the bronchial atresia prenatal diagnosis possible?].
Mechoulan A, Podevin G, Paumier A, Philippe HJ, Le Mouel F, Le Vaillant C, Quéré MP, Joubert M, Winer N. Mechoulan A, et al. Among authors: le mouel f, le vaillant c. Gynecol Obstet Fertil. 2008 Apr;36(4):407-12. doi: 10.1016/j.gyobfe.2007.12.020. Epub 2008 Apr 15. Gynecol Obstet Fertil. 2008. PMID: 18417406 French.
[Acardiac twins: pronostics markers' study].
Barré M, Le Vaillant C, Boog G, Joubert M, Winer N, Philippe H. Barré M, et al. Among authors: le vaillant c. Gynecol Obstet Fertil. 2012 Feb;40(2):93-8. doi: 10.1016/j.gyobfe.2011.08.011. Epub 2011 Nov 17. Gynecol Obstet Fertil. 2012. PMID: 22099976 Review. French.
[When should evoke prenatal paternal uniparental disomy 14?].
Boiffard F, Bénéteau C, Quéré MP, Philippe HJ, Le Vaillant C. Boiffard F, et al. Among authors: le vaillant c. Gynecol Obstet Fertil. 2014 Apr;42(4):254-7. doi: 10.1016/j.gyobfe.2013.09.001. Epub 2014 Jan 3. Gynecol Obstet Fertil. 2014. PMID: 24394322 French.
Blepharophimosis, short humeri, developmental delay and hirschsprung disease: expanding the phenotypic spectrum of MED12 mutations.
Isidor B, Lefebvre T, Le Vaillant C, Caillaud G, Faivre L, Jossic F, Joubert M, Winer N, Le Caignec C, Borck G, Pelet A, Amiel J, Toutain A, Ronce N, Raynaud M, Verloes A, David A. Isidor B, et al. Among authors: le vaillant c, le caignec c. Am J Med Genet A. 2014 Jul;164A(7):1821-5. doi: 10.1002/ajmg.a.36539. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715367
56 results