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The Journal of Clinical Investigation|January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophinK Matsumura, A H Burghes, M Mora, et al.Circulation|September 1, 1996
Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenonD Annane, P Merlet, H Radvanyi, et al.Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2G Collod, M L Chu, T Sasaki, et al.Human Mutation|January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.Human Genetics|January 1, 1984
The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19C Julier, D Weil, P Couillin, et al.Journal of Developmental Origins of Health and Disease|July 24, 2014
Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humansS Mayeur, O Cisse, A Gabory, et al.American Journal of Human Genetics|January 1, 1986
Further evidence for the dispersion of the human fibrillar collagen genesC Huerre-Jeanpierre, M G Mattei, D Weil, et al.Genomics|October 1, 1991
The distal region of 11p13 and associated genetic diseasesM Mannens, J M Hoovers, E M Bleeker-Wagemakers, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1990
Role for the Wilms tumor gene in genital development?V van Heyningen, W A Bickmore, A Seawright, et al.Pageof 24