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Page 1
De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndrome.
Faivre L, Khau Van Kien P, Callier P, Ruiz-Pallares N, Baudoin C, Plancke A, Wolf JE, Thauvin-Robinet C, Durand E, Minot D, Dulieu V, Metaizeau JD, Leheup B, Coron F, Bidot S, Huet F, Jondeau G, Boileau C, Claustres M, Mugneret F. Faivre L, et al. Among authors: bidot s. Eur J Med Genet. 2010 Jul-Aug;53(4):208-12. doi: 10.1016/j.ejmg.2010.05.002. Epub 2010 May 15. Eur J Med Genet. 2010. PMID: 20478419
De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection.
Thevenon J, Callier P, Thauvin-Robinet C, Mejean N, Falcon-Eicher S, Maynadie M, de Maistre E, Bidot S, Huet F, Beri-Dexheimer M, Jonveaux P, Mugneret F, Faivre L. Thevenon J, et al. Among authors: bidot s. Am J Med Genet A. 2011 Jan;155A(1):126-9. doi: 10.1002/ajmg.a.33809. Am J Med Genet A. 2011. PMID: 21204219 No abstract available.
Ocular syphilis and HIV infection.
Biotti D, Bidot S, Mahy S, Buisson M, Duong M, Grappin M, Creuzot-Garcher C, Chavanet P, Piroth L. Biotti D, et al. Among authors: bidot s. Sex Transm Dis. 2010 Jan;37(1):41-3. doi: 10.1097/OLQ.0b013e3181b3e4d8. Sex Transm Dis. 2010. PMID: 20118676
[Iris heterochromia in acquired Horner's syndrome].
Beynat J, Soichot P, Bidot S, Dugas B, Creuzot-Garcher C, Bron A. Beynat J, et al. Among authors: bidot s. J Fr Ophtalmol. 2007 Sep;30(7):e19. doi: 10.1016/s0181-5512(07)91365-0. J Fr Ophtalmol. 2007. PMID: 17878817 French.
Skew deviation and retinal photography.
Biotti D, Bidot S. Biotti D, et al. Among authors: bidot s. Neurology. 2011 Dec 13;77(24):2137. doi: 10.1212/WNL.0b013e31823d7698. Neurology. 2011. PMID: 22170943 No abstract available.
53 results