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Revue Neurologique|November 23, 2007
[Cobalamin metabolism disorders in adult patients]C Thauvin-Robinet, E RozeJournal De Gynecologie, Obstetrique Et Biologie De La Reproduction|April 13, 2010
[Impact of maternal age distribution on the expected live birth prevalence of Down's syndrome in the metropolitan France between 1965 and 2008]T Rousseau, C Ferdynus, C Thauvin-Robinet, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|January 25, 2002
Association of Marfan's syndrome and Turner's syndromeC Thauvin-Robinet, J V De Monléon, A Nivelon-Chevallier, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|May 1, 2010
[Variations in the prevalence of Down's syndrome in the French population between 1978 and 2005]T Rousseau, E Amar, C Ferdynus, et al.Prenatal Diagnosis|July 5, 2001
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephalyC Thauvin-Robinet, T Rousseau, C Durand, et al.International Journal of Oral and Maxillofacial Surgery|September 10, 2018
Diagnostic criteria in Pai syndrome: results of a case series and a literature reviewA Morice, E Galliani, J Amiel, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 25, 2021
Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K-AKT-mTOR signaling pathwayN Bourgon, V Carmignac, A Sorlin, et al.American Journal of Medical Genetics. Part A|August 8, 2006
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterizationP Callier, L Faivre, N Marle, et al.Prenatal Diagnosis|March 28, 2007
Syndromic encephalocele in a fetal case with a 1p35-pter deletion and a 14q32-qter duplication inherited from a maternal balanced translocationC Thauvin-Robinet, P Callier, N Laurent, et al.American Journal of Medical Genetics. Part A|August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndromeP Callier, L Faivre, V Cusin, et al.Pageof 6