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Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.Bioorganic & Medicinal Chemistry Letters|August 8, 2007
A synthetic entry to pladienolide B and FD-895Alexander L Mandel, Brian D Jones, James J La Clair, et al.Nature|February 14, 1991
Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresisA Vincent, D Heitz, C Petit, et al.Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996
A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression patternG Lombard-Platet, S Savary, C O Sarde, et al.American Journal of Human Genetics|May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndromeB Arveiler, G de Saint-Basile, A Fischer, et al.The EMBO Journal|September 5, 2001
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motifC Schaeffer, B Bardoni, J L Mandel, et al.American Journal of Medical Genetics|May 1, 1988
Improved DNA markers for efficient analysis of fragile X familiesR Heilig, I Oberlé, B Arveiler, et al.American Journal of Diseases of Children (1960)|April 1, 1976
Transient bacteremia in pediatric patients after dental extractionW T Speck, S S Spear, E Krongrad, et al.Biochimica Et Biophysica Acta|September 19, 1995
Isolation of cDNA clone encoding human homologue of senescence marker protein-30 (SMP30) and its location on the X chromosomeT Fujita, J L Mandel, T Shirasawa, et al.International Journal of Immunopharmacology|May 1, 1994
Treatment of radiation disease by Nocardia fraction: possible effect of inflammatory cytokinesL Mandel, I Trebichavský, H Tlaskalová, et al.Pageof 31