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	1.	[The 48,XXXX syndrome: study of psychomotor development from birth to 11 years of age and review of the literature]. [electronic resource] by Plauchu, H Ollagnon-Roman, E Armand, J P Robert, J M Producer: 19880829 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Diagnosis of congenital myotonic dystrophy in a neonate: its familial consequences]. [electronic resource] by Lesca, G Haÿs, S Bourgeois, J Bost, M Ollagnon-Roman, E Putet, G Producer: 20030924 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Unilateral presentation of X-linked myotubular myopathy (XLMTM) in two out of three female carriers in a family with no affected male]. [electronic resource] by Drouet, A Ollagnon-Roman, E Streichenberger, N Biancalana, V Cossée, M Guilloton, L Petiot, P Producer: 20080801 In: Revue neurologique vol. 164 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers]. [electronic resource] by Lesca, G Ollagnon-Roman, E Lachanat, J Dusser, A Edery, P Jeanpierre, M Plauchu, H Producer: 20020503 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[X-linked adrenoleukodystrophy in a female proband: clinical presentation, biological diagnosis and family consequences]. [electronic resource] by Lesca, G Vanier, M T Creisson, E Bendelac, N Hainque, B Ollagnon-Roman, E Aubourg, P Producer: 20051025 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias]. [electronic resource] by Lesca, G Demarquay, G Llense, S Streichenberger, N Petiot, P Michel-Calemard, L Récan, D Vial, C Ollagnon-Roman, E Producer: 20031201 In: Revue neurologique vol. 159 Availability: No items available. Save to lists Add to cart (remove)
	7.	Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France Network. [electronic resource] by Sturtz, F G Chauvin, F Ollagnon-Roman, E Bost, M Latour, P Bonnebouche, C Gonnaud, P M Bady, B Chazot, G Vandenberghe, A Producer: 19961119 In: European neurology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. [electronic resource] by Richard, I Brenguier, L Dinçer, P Roudaut, C Bady, B Burgunder, J M Chemaly, R Garcia, C A Halaby, G Jackson, C E Kurnit, D M Lefranc, G Legum, C Loiselet, J Merlini, L Nivelon-Chevallier, A Ollagnon-Roman, E Restagno, G Topaloglu, H Beckmann, J S Producer: 19970603 In: American journal of human genetics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	9.	[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]. [electronic resource] by Humbertclaude, V Hamroun, D Picot, M-C Bezzou, K Bérard, C Boespflug-Tanguy, O Bommelaer, C Campana-Salort, E Cances, C Chabrol, B Commare, M-C Cuisset, J-M de Lattre, C Desnuelle, C Echenne, B Halbert, C Jonquet, O Labarre-Vila, A N'guyen-Morel, M-A Pages, M Pepin, J-L Petitjean, T Pouget, J Ollagnon-Roman, E Richelme, C Rivier, F Sacconi, S Tiffreau, V Vuillerot, C Béroud, C Tuffery-Giraud, S Claustres, M Producer: 20140606 In: Revue neurologique vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)