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FEBS Letters|May 16, 1994
The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane proteinM Contreras, J Mosser, J L Mandel, et al.
Cell Biology International|April 1, 1994
Protective effects of Nocardia delipidated cell mitogen on the mucosa of the small intestine after irradiation of germ-free pigletsH Kozakova, L Mandel, I Trebichavsky, et al.
American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyI Oberlé, D Drayna, G Camerino, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxiaR Fujita, A Hanauer, G Sirugo, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genomics|November 23, 2000
Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: inductibility by retinoic acid and forskolinA Pujol, N Troffer-Charlier, E Metzger, et al.
Nature Genetics|August 1, 1993
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationD Devys, Y Lutz, N Rouyer, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasiaM C Vincent, V Biancalana, D Ginisty, et al.
Biochimica Et Biophysica Acta|June 24, 1983
Similarity of genetic distance determined from DNA thermal denaturation profiles to standard estimates of bacteriophage relatednessA T Ansevin, D L Vizard, M L Mandel, et al.
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