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	1.	[Paraneoplastic syndromes (2)]. [electronic resource] by Lortholary, A Cossee, M Gamelin, E Larra, F Producer: 19940607 In: Bulletin du cancer vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Paraneoplastic syndromes (1)]. [electronic resource] by Lortholary, A Cossee, M Gamelin, E Larra, F Producer: 19940607 In: Bulletin du cancer vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Mental retardation in fragile X syndrome]. [electronic resource] by Mandel, J L Biancalana, V Cossée, M Devys, D Moutou, C Producer: 19961023 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 3 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia. [electronic resource] by Chassaing, N Bourthoumieu, S Cossee, M Calvas, P Vincent, M-C Producer: 20060802 In: Human mutation vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy. [electronic resource] by Echaniz-Laguna, A Rousso, E Anheim, M Cossée, M Tranchant, C Producer: 20060120 In: Neurology vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestor. [electronic resource] by Zühlke, C Laccone, F Cossée, M Kohlschütter, A Koenig, M Schwinger, E Producer: 19980925 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy]. [electronic resource] by Echaniz-Laguna, A Rousso, E Anheim, M Fleury, M Cossée, M Tranchant, C Producer: 20050929 In: Revue neurologique vol. 161 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	G130V, a common FRDA point mutation, appears to have arisen from a common founder. [electronic resource] by Delatycki, M B Knight, M Koenig, M Cossée, M Williamson, R Forrest, S M Producer: 19991110 In: Human genetics vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Miyoshi-like distal myopathy with mutations in anoctamin 5 gene. [electronic resource] by Bouquet, F Cossée, M Béhin, A Deburgrave, N Romero, N Leturcq, F Eymard, B Producer: 20120710 In: Revue neurologique vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	[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)
	11.	Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations. [electronic resource] by Cossée, M Schmitt, M Campuzano, V Reutenauer, L Moutou, C Mandel, J L Koenig, M Producer: 19970805 In: Proceedings of the National Academy of Sciences of the United States of America vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Phenotype in X chromosome rearrangements: pitfalls of X inactivation study. [electronic resource] by Schluth, C Cossée, M Girard-Lemaire, F Carelle, N Dollfus, H Jeandidier, E Flori, E Producer: 20070504 In: Pathologie-biologie vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Kennedy's Disease Initially Manifesting as an Endocrine Disorder. [electronic resource] by Battaglia, F Le Galudec, V Cossee, M Tranchant, C Warter, J M Echaniz-Laguna, A Producer: 20121002 In: Journal of clinical neuromuscular disease vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation. [electronic resource] by Cossée, M Puccio, H Gansmuller, A Koutnikova, H Dierich, A LeMeur, M Fischbeck, K Dollé, P Koenig, M Producer: 20000623 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	[Update on Bardet-Biedl syndrome]. [electronic resource] by Dollfus, H Verloes, A Bonneau, D Cossée, M Perrin-Schmitt, F Brandt, C Flament, J Mandel, J-L Producer: 20051026 In: Journal francais d'ophtalmologie vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Clinical and genetic abnormalities in patients with Friedreich's ataxia. [electronic resource] by Dürr, A Cossee, M Agid, Y Campuzano, V Mignard, C Penet, C Mandel, J L Brice, A Koenig, M Producer: 19970123 In: The New England journal of medicine vol. 335 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13. [electronic resource] by Montermini, L Rodius, F Pianese, L Moltò, M D Cossée, M Campuzano, V Cavalcanti, F Monticelli, A Palau, F Gyapay, G Producer: 19951130 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	18.	Correlation between left ventricular hypertrophy and GAA trinucleotide repeat length in Friedreich's ataxia. [electronic resource] by Isnard, R Kalotka, H Dürr, A Cossée, M Schmitt, M Pousset, F Thomas, D Brice, A Koenig, M Komajda, M Producer: 19970605 In: Circulation vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits. [electronic resource] by Puccio, H Simon, D Cossée, M Criqui-Filipe, P Tiziano, F Melki, J Hindelang, C Matyas, R Rustin, P Koenig, M Producer: 20010315 In: Nature genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T). [electronic resource] by Oestergaard, S T Stojkovic, T Dahlqvist, J R Bouchet-Seraphin, C Nectoux, J Leturcq, F Cossée, M Solé, G Thomsen, C Krag, T O Vissing, J Publication details: Neurology. Genetics Dec 2016 In: Neurology. Genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 31 results.