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Bulletin De La Societe De Pathologie Exotique (1990)|March 3, 2012
[Reality of healthcare access for migrant children in Mayotte]J Baillot, B Luminet, N Drouot, et al.
Cerebellum (London, England)|June 4, 2013
The Salih ataxia mutation impairs Rubicon endosomal localizationM Assoum, M A Salih, N Drouot, et al.
European Journal of Endocrinology|March 29, 2001
Identification of a novel mutation in the autoimmune regulator (AIRE-1) gene in a French family with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophyP Saugier-Veber, N Drouot, L M Wolf, et al.
Cancer Research|June 13, 2000
Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragmentsF Charbonnier, G Raux, Q Wang, et al.
Nature|March 14, 1996
A comprehensive genetic map of the human genome based on 5,264 microsatellitesC Dib, S Fauré, C Fizames, et al.
Brain : a Journal of Neurology|May 2, 2007
A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23M Gribaa, M Salih, M Anheim, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Genome Research|December 10, 1998
Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14qC Paternotte, D Rudnicki, C Fizames, et al.
Journal of Neurology|August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arraysD H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Brain : a Journal of Neurology|August 22, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patientsM Anheim, B Monga, M Fleury, et al.
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