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Page 1
Detection of TRIM32 deletions in LGMD patients analyzed by a combined strategy of CGH array and massively parallel sequencing.
Nectoux J, de Cid R, Baulande S, Leturcq F, Urtizberea JA, Penisson-Besnier I, Nadaj-Pakleza A, Roudaut C, Criqui A, Orhant L, Peyroulan D, Ben Yaou R, Nelson I, Cobo AM, Arné-Bes MC, Uro-Coste E, Nitschke P, Claustres M, Bonne G, Lévy N, Chelly J, Richard I, Cossée M. Nectoux J, et al. Among authors: bonne g. Eur J Hum Genet. 2015 Jul;23(7):929-34. doi: 10.1038/ejhg.2014.223. Epub 2014 Oct 29. Eur J Hum Genet. 2015. PMID: 25351777 Free PMC article.
Emery-Dreifuss muscular dystrophy.
Helbling-Leclerc A, Bonne G, Schwartz K. Helbling-Leclerc A, et al. Among authors: bonne g. Eur J Hum Genet. 2002 Mar;10(3):157-61. doi: 10.1038/sj.ejhg.5200744. Eur J Hum Genet. 2002. PMID: 11973618 Review.
LMNA mutations in atypical Werner's syndrome.
Bonne G, Levy N. Bonne G, et al. Lancet. 2003 Nov 8;362(9395):1585-6; author reply 1586. doi: 10.1016/S0140-6736(03)14761-7. Lancet. 2003. PMID: 14615129 No abstract available.
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].
Ben Yaou R, Bécane HM, Demay L, Laforet P, Hannequin D, Bohu PA, Drouin-Garraud V, Ferrer X, Mussini JM, Ollagnon E, Petiot P, Penisson-Besnier I, Streichenberger N, Toutain A, Richard P, Eymard B, Bonne G. Ben Yaou R, et al. Among authors: bonne g. Rev Neurol (Paris). 2005 Jan;161(1):42-54. doi: 10.1016/s0035-3787(05)84972-0. Rev Neurol (Paris). 2005. PMID: 15678000 French.
[Cardiac manifestations of laminopathies].
Brette S, Penisson-Besnier I, Dupuis JM, Bonne G, Victor J. Brette S, et al. Among authors: bonne g. Arch Mal Coeur Vaiss. 2004 Oct;97(10):973-7. Arch Mal Coeur Vaiss. 2004. PMID: 16008174 French.
244 results