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Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect.
Jaillard S, Loget P, Lucas J, Dubourg C, Le Bouar G, Demurger F, Bertorello I, David V, Poulain P, Odent S, Belaud-Rotureau MA. Jaillard S, et al. Among authors: odent s. Eur J Med Genet. 2011 Mar-Apr;54(2):186-8. doi: 10.1016/j.ejmg.2010.11.001. Epub 2010 Nov 27. Eur J Med Genet. 2011. PMID: 21115145
Remarks about the prognosis in case of antenatal diagnosis of gastroschisis.
Poulain P, Milon J, Frémont B, Proudhon JF, Odent S, Babut JM, Le Marec B, Grall JY, Giraud JR. Poulain P, et al. Among authors: odent s. Eur J Obstet Gynecol Reprod Biol. 1994 May 18;54(3):185-90. doi: 10.1016/0028-2243(94)90280-1. Eur J Obstet Gynecol Reprod Biol. 1994. PMID: 7926232 Review.
[Reflections on 10 years of medically induced abortions in Ille-et-Vilaine].
Schneider S, Roussey M, Odent S, Debroise C, Poulain P, Jouan H, Milon J, Betremieux P, Journel H, Le Mee F, et al. Schneider S, et al. Among authors: odent s. J Gynecol Obstet Biol Reprod (Paris). 1994;23(2):157-65. J Gynecol Obstet Biol Reprod (Paris). 1994. PMID: 8040573 French.
Opitz GBBB syndrome: chromosomal evidence of an X-linked form.
Verloes A, David A, Odent S, Toutain A, André MJ, Lucas J, Le Marec B. Verloes A, et al. Among authors: odent s. Am J Med Genet. 1995 Oct 23;59(1):123-8. doi: 10.1002/ajmg.1320590124. Am J Med Genet. 1995. PMID: 8849003
Features of DiGeorge syndrome and CHARGE association in five patients.
de Lonlay-Debeney P, Cormier-Daire V, Amiel J, Abadie V, Odent S, Paupe A, Couderc S, Tellier AL, Bonnet D, Prieur M, Vekemans M, Munnich A, Lyonnet S. de Lonlay-Debeney P, et al. Among authors: odent s. J Med Genet. 1997 Dec;34(12):986-9. doi: 10.1136/jmg.34.12.986. J Med Genet. 1997. PMID: 9429139 Free PMC article.
376 results