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Human Genetics|August 4, 2005
Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardationK Poirier, J Abriol, I Souville, et al.Human Genetics|March 1, 1988
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD geneJ J Pernelle, P Chafey, J Chelly, et al.Human Molecular Genetics|August 11, 1999
Doublecortin, a stabilizer of microtubulesD Horesh, T Sapir, F Francis, et al.Genomics|July 1, 1994
Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) miceA M George, V Reed, P Glenister, et al.American Journal of Medical Genetics|May 8, 2000
X-linked congenital ataxia: a clinical and genetic studyE Bertini, V des Portes, G Zanni, et al.American Journal of Medical Genetics|July 9, 1999
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)L B Jemaa, V des Portes, R Zemni, et al.Biotechniques|March 5, 2003
DHPLC-based method for DNA methylation analysis of differential methylated regions from imprinted genesP Couvert, K Poirier, A Carrié, et al.Annales De Genetique|May 26, 1998
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11S C Deqaqi, M N'Guessan, J Forner, et al.Genomics|October 1, 1989
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophiesH Gilgenkrantz, J Chelly, M Lambert, et al.Human Genetics|October 1, 1986
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyJ Chelly, F Marlhens, B Le Marec, et al.Pageof 14