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Pediatrie|January 1, 1993
[Rapid diagnosis of tuberculous meningitis by polymerase chain reaction. A case in an infant]S Odent, J Minet, R Lelièvre, et al.Human Mutation|March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. OnlineC Dubourg, S Odent, P Fergelot, et al.Clinical Genetics|August 1, 1988
Genetic counselling in a case of TAR syndrome where the father presented malformations of the feetB Le Marec, S Odent, H Bracq, et al.Annales De Genetique|January 1, 1988
[Oto-palato-digital type I syndrome in five generations. Relationship to the type II form]B Le Marec, S Odent, E Bracq, et al.European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.Pediatrie|January 1, 1993
[Value and limits of autopsy in perinatal medicine. A plea for complete perimortem evaluation]P Bétrémieux, P Pladys, P Poulain, et al.Annales De Biologie Clinique|January 9, 2004
[Genetic study of holoprosencephaly]C Dubourg, L Lazaro, M Blayau, et al.Annales D'Endocrinologie|February 15, 2002
[Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation]C Derrien, S Odent, C Henry, et al.American Journal of Medical Genetics|August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndromeS Briault, S Odent, J Lucas, et al.Pediatrie|January 1, 1993
[Diffuse subcortical heterotopias of the gray matter]C Treguier, P Muh, C Le Berre, et al.Pageof 11