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Annales De Genetique|January 1, 1988
[The 48,XXXX syndrome: study of psychomotor development from birth to 11 years of age and review of the literature]H Plauchu, E Ollagnon-Roman, J P Armand, et al.Revue Neurologique|March 25, 2008
[Unilateral presentation of X-linked myotubular myopathy (XLMTM) in two out of three female carriers in a family with no affected male]A Drouet, E Ollagnon-Roman, N Streichenberger, et al.Annales De Genetique|October 20, 1999
CTG instability in myotonic dystrophy: molecular genetic analysis of families from south-eastern France with characteristics of intergenerational variation in CGT repeat numbersS Duthel, M Bost, E Ollagnon, et al.Human Mutation|April 29, 1999
Characterisation of 16 polymorphic markers in the NF2 gene: application to hemizygosity detectionP Legoix, M F Legrand, E Ollagnon, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 5, 2001
[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers]G Lesca, E Ollagnon-Roman, J Lachanat, et al.Journal De Genetique Humaine|August 1, 1987
[Renal hypoplasia, polydactyly, cardiopathy: a new syndrome?]J Bonnet, M P Cordier, E Ollagnon, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 10, 2005
[X-linked adrenoleukodystrophy in a female proband: clinical presentation, biological diagnosis and family consequences]G Lesca, M T Vanier, E Creisson, et al.Journal De Genetique Humaine|May 1, 1987
[Female pseudohermaphroditism associated with cloacal dysgenesis]M P Cordier, E Ollagnon, M H Guillaud, et al.Revue Neurologique|September 19, 2003
[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias]G Lesca, G Demarquay, S Llense, et al.Human Mutation|January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1BP Latour, F Blanquet, E Nelis, et al.Pageof 2