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Current Genetics|March 1, 1990
Cloning and expression of a hybrid Streptomyces clavuligerus cefE gene in Penicillium chrysogenumC A Cantwell, R J Beckmann, J E Dotzlaf, et al.
Circulation Research|July 1, 1992
Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French familiesK Schwartz, J Beckmann, C Dufour, et al.
Journal of Medical Genetics|April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.
Genomics|July 15, 1994
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneityM Medhioub, D Cherif, F Benessy, et al.
American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Neurology|November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.
Plos One|October 12, 2013
Indoor navigation by people with visual impairment using a digital sign systemGordon E Legge, Paul J Beckmann, Bosco S Tjan, et al.
Journal of the American College of Cardiology|August 1, 1997
Primary pulmonary hypertension: improved long-term effects and survival with continuous intravenous epoprostenol infusionS M Shapiro, R J Oudiz, T Cao, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|April 19, 2011
Fracture prevention by femoroplasty--cement augmentation of the proximal femurJ Beckmann, R Springorum, E Vettorazzi, et al.
Brain : a Journal of Neurology|February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion IslandM Fardeau, D Hillaire, C Mignard, et al.
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