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Page 1
Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities.
Scala M, Khan K, Beneteau C, Fox RG, von Hardenberg S, Khan A, Joubert M, Fievet L, Musquer M, Le Vaillant C, Holsclaw JK, Lim D, Berking AC, Accogli A, Giacomini T, Nobili L, Striano P, Zara F, Torella A, Nigro V, Cogné B, Salick MR, Kaykas A, Eggan K, Capra V, Bézieau S, Davis EE, Wells MF. Scala M, et al. Among authors: le vaillant c. Genet Med. 2024 Apr;26(4):101057. doi: 10.1016/j.gim.2023.101057. Epub 2023 Dec 27. Genet Med. 2024. PMID: 38158856 Free article.
[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.
Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases.
Allaf B, Dreux S, Schmitz T, Czerkiewicz I, Le Vaillant C, Benachi A, Houfflin-Debarge V, Maréchaud M, Oury JF, Muller F. Allaf B, et al. Among authors: le vaillant c. Prenat Diagn. 2015 Dec;35(13):1331-5. doi: 10.1002/pd.4700. Epub 2015 Nov 3. Prenat Diagn. 2015. PMID: 26426702
[Management of premature rupture of the membranes at term: how long to delay? Results of a prospective multicentric study in 713 cases].
Seince N, Biquard F, Sarfati R, Barjot P, Foucher F, Lassel L, Levaillant C, M'Bwang Seppoh R, Perrotin F, Rachedi N, Guérin O, Pierre F, Descamps P. Seince N, et al. J Gynecol Obstet Biol Reprod (Paris). 2001 Feb;30(1):42-50. J Gynecol Obstet Biol Reprod (Paris). 2001. PMID: 11240504 Free article. Clinical Trial. French.
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.
[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